5 MAY BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ENTOMOLOGY VOL. XVI 1965 BRITISH MUSEUM (NATURAL HISTORY) LONDON: 1966 DATES OF PUBLICATION OF THE PARTS No. i • •' 3 June 1965 No. 2 23 August 1965 No. 3 ..... 23 August 1965 No. 4 ..... 25 October 1965 PRINTED IN GREAT BRITAIN BY ADLARD & SON LIMITED BARTHOLOMEW PRESS, DORKING CONTENTS 5 MAY ENTOMOLOGY VOLUME XVI No. i. Diptera from Nepal. Bibionidae. By D. ELMO HARDY Agromyzidae. By K. A. SPENCER PAGE i 25 No. 2. A systematic revision of the Ameniinae (Diptera : Calliphoridae) . By R. W. CROSSKEY 33 No. 3. A revision of the Nodini and a key to the genera of Eumolpidae of Africa (Coleoptera : Eumolpidae). By B. J. SELMAN 141 No. 4. On some Coccidae (Homoptera), chiefly from Africa. By G. DE LOTTO 175 Index to Volume XVI 241 DIPTERA FROM NEPAL BIBIONIDAE D. ELMO HARDY AGROMYZIDAE K. A. SPENCER BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ENTOMOLOGY Vol. 16 No. i LONDON: 1965 DIPTERA FROM NEPAL BIBIONIDAE BY D. ELMO HARDY Department of Entomology, University of Hawaii AGROMYZIDAE BY K. A. SPENCER 19, Redington Road, Hampstead, London, I^ngland Pp. 1-31 ; 61 Text-figures BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ENTOMOLOGY Vol. 16 No. i LONDON: 1965 THE BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY), instituted in 1949, is issued in five series corresponding to the Departments of the Museum, and an Historical Series. Parts will appear at irregular intervals as they become ready. Volumes will contain about three or four hundred pages, and will not necessarily be completed within one calendar year. This paper is Vol. 16, No. I of the Entomological series. The abbreviated titles of periodicals cited follow those of the World List of Scientific Periodicals. Trustees of the British Museum (Natural History) 1965 TRUSTEES OF THE BRITISH MUSEUM (NATURAL HISTORY) Issued 3 June, 1965 Price Fifteen Shillings DIPTERA FROM NEPAL BIBIONIDAE1 By D. ELMO HARDY SYNOPSIS This study is based upon sixty-one specimens collected by Ralph L. Coe, British Museum (Natural History) 1961-62 expedition to Nepal, and seventeen specimens collected by L. W. Swan, American expeditions to Nepal 1954 and 1960. The collections contained twelve species in four genera of Bibionidae. Six of the species are apparently undescribed and ten are new records for Nepal. One additional species, Penthetria indica (Brunetti), has been recorded from Nepal but was not represented in the collections. THIS most valuable collection gives us considerable insight into a previously almost entirely unknown fauna and adds materially to our knowledge of the Bibionidae of the Oriental region. I am indebted to Ralph L. Coe for the privilege of studying the material from the British Museum collection and to Dr. Edward Kessel and Paul Arnaud for the loan of specimens from the California Academy of Sciences. I am also grateful to Mrs. Rogene Radner for preparing the illustrations. TAXONOMIC ARRANGEMENT OF THE KNOWN BIBIONIDAE OF NEPAL Subfamily Pleciinae Subfamily Bibioninae Penthetria atra (Brunetti) Bibio ablusus n. sp. P. indica (Brunetti)* B. affiniproximus n. sp. P. japonica Wiedemann B. capitaneus n. sp. Plecia mallochi Hardy ? $ B. nigerrimus Duda P. sp. ? $ impostor complex B. scaurus n. sp. B. totonigra n. sp. Dilophus gratiosus Bigot D. hirsutus n. sp. *Not present in this collection. KEY TO KNOWN SPECIES OF BlBIONIDAE FROM NEPAL 1 Front tibia lacking spines or spurs. Vein R2+3 present (Text-fig. 3). Pleciinae . 2 Front tibia with large apical spurs (Text-fig. 1 1 ) or with a ring of spines at the apex and a row of four spines across the middle (Text-fig. 46) . Bibioninae ... 6 2 Vein R2+3 short, oblique or vertical in position (Text-fig. 6) . Plecia Wiedemann . 3 Vein R2+3 elongate, almost horizontal in position (Text-fig. 3). Penthetria Meigen . 4 3 Thorax entirely rufous . . . Plecia mallochi Hardy (and related species) Pleura black, front margin of mesonotum dark coloured Plecia impostor Brunetti complex 4 At least posterior half of mesonotum bright orange ...... 5 Entirely black species ....... Penthetria atra (Brunetti) 1Published with the approval of the Director of the Hawaii Agricultural Experiment Station as Technical Paper No. 694. Bull. Brit. Mus. (Nat. Hist.), Ent. 16 (i), 1965. 4 D. ELMO HARDY 5 Anterior portion of mesonotum black .... P. japonica Wiedemann Mesonotum entirely rufous ....... P. indica (Brunetti) 6 Front tibia with a row of apical spines and with four spines across the middle (Text- fig. 46). Dilophus Meigen .'........ 7 Front tibia with apical spurs. Bibio Geoffrey . ... . . . . 8 7 Basal section of radial sector very short, about one-fifth as long as the r-m crossvein (Text-fig. 50) . Body and legs densely black pilose. Spines of front tibia arranged as in Text-fig. 49 ........ D. hirsutus n. sp. Basal section of radial sector nearly one-half as long as r-m (Text-fig. 47) . Body and legs sparsely yellow pilose. Spines of front tibia arranged as in Text-fig. 46 D. gratiosus Bigot 8 Spurs of front tibia sharp pointed (Text-figs. 18 and 22) ..... 9 Outer spur of front tibia rounded, blunt at apex (best seen from lateral view) (Text- fig. 30). Ninth tergum of male with a U-shaped hind margin (Text-fig. 33). An- tenna lo-segmented. Large subopaque black species . B. nigerrimus Duda 9 Wings entirely hyaline, except for the stigma ; posterior veins colorless . . 10 Wings distinctly infuscated, darker on the anterior margin ; posterior veins darker than the membrane ........... 1 1 10 Large species, male body 15-5 mm. ; wings 14-0 mm. Crossvein r-m less than half as long as the base of the Rs (Text-fig. 25). Last segment of palpus six times longer than wide (Text-fig. 23). . . . . . . B. capitaneus n. sp. Small species, body 5-0 mm. ; wings 4-6 mm. Crossvein v-m equal in length to the base of Rs. Last segment of palpus scarcely longer than wide (Text-fig. 14) B. affiniproximus n. sp. 11 Hind basitarsi of male not swollen ; wings evenly fumose, not spotted . . 12 Hind basitarsi of male swollen (Text-fig. 35). Female with brown spots on the wings as in Text-fig. 37 ........ B. scaurus n. sp. 12 Inner spur well developed, subequal to outer (Text-fig. 42). Body entirely black pilose. Wings smoky black, costal cell and stigma black. Last segment of palpus elongate, 6-7 times longer than wide. Crossvein r-m approximately equal to the base of Rs (Text-fig. 40). . . . . . B. totonigra n. sp. — Inner spur of front tibia rudimentary, very small compared to the outer (Text-fig. 1 1 ) . Body predominantly yellow pilose. Wings lightly fumose, costal cell brownish yellow, stigma brown. Last segment of palpus short, scarcely longer than wide. Crossvein r-m about one-half as long as basal section of Rs (Text-fig. 9) B. ablusus n. sp. Subfamily PLECIINAE Genus PENTHETRIA Meigen Penthetria Meigen, 1803, Illiger's Mag. 2 : 264. Threneste Wiedemann, 1830, Aussereurop. zweifl. Ins. 2 : 618 (refer to Edwards, 1928 : 683). Eupeitenus Macquart, 1838, Dipt. exot. nouv. ou pen connus 1 : 85. Crapitula Gimmerthal, 1845, Bull. Soc. Nat. Moscou, 18 : 330. Pleciomyia Brunetti, 1911, Rec. Indian Mus. 4 : 269. Parapleciomyia Brunetti, 1912, Rec. Indian Mus. 7 : 446. The members of this genus differ from Plecia by having vein R2+3 elongate and horizontal in position, almost parallel to vein -R4+5, and the claspers of the male genitalia lateral in position and large and conspicuous. Three species have been recorded from Nepal, two of these (P. atra (Brunetti) and japonica Wiedemann) are present in this collection. P. indica (Brunetti) was recorded by Brunetti (1911 : 272). Type species : Penthetria holosericea Meigen. DIPTERA FROM NEPAL 5 Penthetria atra (Brunetti) (Text-figs. 1-4) Plecia atra Brunetti, 1911, Rec. Indian Mus. 4 : 272. To date only female specimens of atra have been recorded. It is readily recognized from all other known Penthetria from this region by its entirely black coloration. I have on hand a male specimen from Sze-chuan, China, which appears to be this species. It is highly probable, however, that a complex of species may have the same general appearance and it would not be practical to describe this male as atra. $. Entirely black species covered with short black setae over the body and legs. The head is short and broad. The rostrum is not developed and the front has a prominent tubercle on the lower median portion. As seen in dorsal view the head is as in Text-fig. 2. The antennae are twelve-segmented (Text-fig, i) ; Brunetti, in the original description, indicated this, but his figure (1912, plate 12, fig. 16) shows only eleven segments with an indication of two segments being present in the first joint of the flagellum. The wings are entirely smoky black. The venation is as in Text-fig. 3. The forking of veins MT and M2 is well beyond the r-m crossvein. The female genitalia are as in Text-fig. 4. Brunetti recorded the length of this species as 8-0-12-0 mm. The specimens at hand measure 9-5 mm. for the body and 10-0 mm. for the wings. Brunetti's type-series was from Bhim Tal, KUMAON, western Himalayas and from Soondrijal, NEPAL. Type in the Indian Museum. NEPAL : Taplejung Distr., Sangu, c. 6,200', bamboo plantation, i $, n. x. 1961 ; by rocky stream, I $, 7-16. x. 1961 ; and mixed vegetation by stream in valley, i ?, ix-x. 1961 (R. L. Coe), B.M. (N.H.). Penthetria indica (Brunetti) Plecia indica Brunetti, 1911, Rec. Indian Mus. 4 : 271. Type locality, Darjeeling. Evidently widely distributed through northern India and Nepal. Brunetti recorded cotypes from Soondrijal, Nepal. Type in the Indian Museum. This species was not present in the collection of the British Museum from Nepal. P. indica is differentiated from other Penthetria known from this section of the world by having the mesonotum entirely rufous, also by the comparatively short vein R2+3. The following notes were made from a $ specimen from INDIA ; United Province, Naini Tal, 6,750', 25. ii. 1934 (/. A. Graham), B.M. (N.H.). The entire dorsum of the thorax is opaque orange except for the apex of the scutellum, which is shiny black. The remainder of the body and all appendages are black ; the pleura and femora have a faint brownish to reddish tinge in the ground colour. The mesonotum is sparsely covered with short yellow hairs. As seen from a dorsal view the head is slightly wider than long, the rostrum is not well developed. The ocellar tubercle is well developed and a rather prominent tumescence is present just above the antennae in the middle of the front. The antennae are twelve-segmented. The leg joints are slender, the hind basitarsus is about one-third as long as the tibia. The pile of the coxae and femora is short, yellow, and the tibiae have short yellow pile with some brown to black pile intermixed. The tarsi are covered with brown to black pile. The wings are smoky brown, darker along the anterior margin. The stigma is dark brown, scarcely darker than the membrane. Vein R2+3 is about equal in length to the distance from the r-m crossvein to the forking of veins R2+3 and /?4 + 5. In this respect 6 D. ELMO HARDY this species is somewhat Plecia-like but vein R2+3 extends almost parallel to #4+5 and in this respect would fit Penthetria. The fork of veins M\ and M2 is situated well before the forking of veins R2+3 and Rt+&. Length (of the specimen studied) : Body, 8-5 mm.; wings, 10-3 mm. Brunetti in the original gave the length as 6-9 mm. 0.7 mm. 4.0mm. FIGS. 1-4. Penthetria atra (Brunetti). Fig. i, antenna ; Fig. 2, head of $, dorsal ; Fig. 3, wing ; Fig. 4, § genitalia, ventral. FIG. 5. Penthetria japonica Wiedemann, section of wing showing branching of M^ and Mz. FIG. 6. Plecia mallochi Hardy?, anterior margin of wing showing fork of radial sector. Penthetria japonica Wiedemann (Text-fig. 5) Penthetria japonica Wiedemann, 1830, Aussereurop. zweifl. Ins. 2 : 618. Plecia ignicollis Walker, 1848, List Dipt. Ins. Brit. Mus. 1 : 116. For a discussion of this synonymy refer to Hardy (1956 : 85) and to Hardy and Takahashi (1960 : 390). As discussed in the latter reference, P. japonica has been commonly treated in the literature as a synonym of P. melanaspis Wiedemann ; however, the male claspers are rather strongly curved downward, rather blunt at their apices in japonica and are straight-sided, rather sharply pointed at the apices DIPTERA FROM NEPAL 7 in melanaspis. Refer to figures 2 C-D and 3A in Hardy and Takahashi (1960 : 390 and 392). This has been treated by Brunetti : (1911 : 270; and 1912 : 161) as Pleciomyia melanaspis Wied. P. japonica also resembles motschulskii (Gimmerthal) , from northern China, Siberia and Sakhalin but the wing venation is distinctly different. In japonica vein Mx is joined directly to the r-m crossvein (Text-fig. 5) and not joined with M2 beyond this crossvein, in motschulskii vein M 1+2 extends well beyond the r-m cross- vein. Also the genitalia are very different in the two species. P. motschulskii has the claspers greatly thickened and blunt (fig. 38, Hardy and Takahashi 1960 : 392). P. japonica is readily recognized from other known Penthetria in Nepal or northern India by having the posterior portion of the mesonotum orange to rufous and the anterior portion velvety black. The remainder of the body and appendages, including the wings, is entirely black. For a more adequate description, refer to Hardy and Takahashi (1960 : 390-391). Length of male : Body and wing, 9-0-10-0 mm. Length of female : Body, 10-0-10-7 mm. ; wings, 7-0-12-0 mm. Type locality : JAPAN. Type in the Zoologisches Museum, Humboldt Universitat, Berlin. I have studied specimens of this species from a wide range of localities throughout NORTHERN INDIA, CHINA, and FORMOSA, as well as JAPAN. NEPAL, Taplejung Distr., Sangu, c. 6,200', mixed vegetation by stream in gully, i , ix. -x. 1961 (R. L. Coe), B.M. (N.H.). Three specimens, two <$ and one $, are in the California Academy of Sciences collection from NEPAL : Manga Deorali, 5,500', 7. xi. 1960 (L. Swan) ; Chyaubas to Risingo, 4,000', no date given — no doubt x. or xi. 1960 (L. Swan) ; and Pass Camp near Tarebhir, 4,500', 26. x. 1960 (L. Swan}. Brunetti (1912 : 161) recorded this species as Pleciomyia melanaspis (Wiedemann), from Soondrijal and Katmandu, Nepal. Genus PLECIA Wiedemann Plecia Wiedemann, 1828, Aussereurop. zweifl. Ins. 1 : 72. Members of this genus are differentiated from Penthetria by the short, almost vertical, vein 7?2+3 (Text-fig. 6) and by the vertical, comparatively small, claspers of the male. Two species are present from Nepal. Both are represented only by females and positive identification is impossible without the males. Type species : Hirtea fulvicollis Fabricius. Plecia sp. ? $ impostor complex One female specimen of the Plecia impostor complex is in the California Academy of Sciences collection from NEPAL : Chyaubas to Risingo, 4,000', no date given — probably collected x. or xi. 1960 (L. Swan). It is impossible to identify species of this complex without the males. The group is characterized by having the meso- notum rufous except for a brown marking on the anterior portion. For a revision of the known Oriental species refer to Hardy 1953. 8 D. ELMO HARDY Plecia mallochi Hardy ? (Text-fig. 6) Penthetria thoracica Gu£rin-M£neville, 1833, in BeUanger, Voy. Indes Orientales, : 507. Paris. [Preoccupied by Laphria thoracica Fabricius, 1805, System. Antl.: 163, a synonym of Plecia collar is (Fabricius)]. Plecia confusa Malloch, 1928, Proc. Linn. Soc. N.S. Wales, 53 : 605, nee P. confusa Loew. Plecia mallochi Hardy, 1948, /. Kans. ent. Soc. 21 : 36. [Change of name for P. confusa Malloch, preoccupied by P. confusa Loew, 1858, Berl. ent. Z. 2 : 109.] Plecia dispersa Hardy, 1958 : 196. [This was presented as a new name for mallochi but the latter is available to replace thoracica Gu6rin-M£neville.] The Plecia which have the thorax entirely rufous have been commonly treated in the literature under the name fulvicollis (Fabricius). Brunetti (1912 : 163) treated Penthetria thoracica Guerin ( = mallochi Hardy), Plecia dorsalis Walker and Plecia subvariens Walker as synonyms under fulvicollis. It is probable that none of these are actually synonyms. Brunetti's concept was based entirely upon colour and obviously included an assortment of species. The species from Nepal may probably be P. mallochi, which was described from Coromandel, S. E. India, but as I have recorded (Hardy, 1958 : 197) it is one of the common species of India and Ceylon. One $ from NEPAL : Arun Valley, below Tumlingtar, River Sabhaya, west shore, c. 1,800', 2i.xii.i962. (R. L. Coe), B.M. (N.H.), appears to be this species, but it cannot be positively identified without the male. The specimen is larger than any mallochi which I have previously seen : the body measures 9-0 mm. and the wing 12-5 mm. although females of mallochi will range to 8-5 mm. for the body and approximately n-o mm. for the wing and this difference is insignificant. P. mallochi is related to javensis Edwards because of the poorly developed ocellar triangle of the male and is differentiated by the broad blunt claspers and the differ- ences in the shape and development of the ninth sternum and tergum of the male. Refer to Hardy (1958 : 196-197 — under P. dispersa) for descriptive details and figures. Genus BIBIO Geoffrey Bibio Geoffroy, 1764, Hist. Nat. Insectes, 2 : 571. Pullata Harris, 1776, Expos. Eng. Ins. : 76. , Hirtea Fabricius, 1798, Ent. Syst., Suppl., : 551 (nee Scopoli, 1763). Bibiophus Bollow, 1954, Z. PflBau 5 (5) : 209, 211. This genus is characterized by the development of strong apical spurs on the front tibiae (Text-fig, n), and by the simple radial sector, with the basal portion equal to or longer than the r-m cross vein. Bibio are rather conspicuously hairy flies, the antennae are short, the segments are thick and closely compressed. Six species of Bibio are known to occur in Nepal, only one of these, B. nigerrimus Duda, has been previously recorded. The other five are apparently undescribed. Type species : Tipula hortulana Linnaeus. DIPTERA FROM NEPAL 9 Bibio ablusus n. sp. (Text-figs. 7-13) This species appears to be related to B. totonigra n. sp. but differs by having the body predominantly yellow pilose ; the wings lightly fumose ; the r-m crossvein short, about one-half as long as the basal section of Rs ; and the terminal segment of the palpus short. 0 7mm. 35mm. FIGS. 7-13. Bibio ablusus n. sp. Fig. 7, $ head, lateral ; Fig. 8, $ head, dorsal ; Fig. 9, wing ; Fig. 10, hind leg, , NEPAL : Taplejung Distr., damp evergreen oak forest above Sangu, c. 8,500-9,200', 2-26. xi. 1961 (R. L. Coe), in the British Museum (Natural History). Bibio totonigra n. sp. (Text-figs. 40-44) This species superficially resembles B. nigerrimus Duda because of the all-black body and appendages and the smoky black wings. The two are not related however, and totonigra is readily differentiated by the slender spurs at the apices of the front tibiae ; by having the r-m crossvein almost equal in length to the basal section of the radial sector ; as well as by many other details. In the key it fits near ablusus n. sp. but is differentiated by the elongate terminal segment of the palpus, the all black pile, smoky black wings, and other characters. cJ. Entirely black species with the body and appendages covered with black pile. Head : The rostrum is not developed, the front margin of the head is not produced beyond the eye margins. The antennae are eleven-segmented, the apical two are closely joined (Text-fig. 41). The apical segment of each palpus is slender, slightly longer than the preapical segment, and six or seven times longer than wide. Thorax : The lower portion of each sternopleuron is polished black, the pleura are otherwise subshining, finely rugose. The mesonotum is pre- DIPTERA FROM NEPAL 19 dominantly opaque black with long black pile on the margins and down each dorsocentral line and is rather coarsely rugose down the median portion and on the sides. The scutellum and metanotum are polished black. Legs : Entirely shining black, densely black haired. The inner spur on the front tibia is about three-fourths as long as the outer (Text-fig. 42). It should be noted that the left front tibia of the type is abnormal. This segment is considerably shrivelled, 40 4.0 mm. . 7 5 mm. 42 44 i 75mm. FIGS. 40-44. Bibio totonigra n .sp. Fig. 40, wing ; Fig. 41, antenna ; Fig. 42, front tibia ; Fig. 43, ninth tergum of $ ; Fig. 44, <$ genitalia, ventral. much shorter than normal and the inner spur is rather poorly developed. The normal develop- ment of the more elongate inner spur is borne out by the second specimen at hand. This speci- men was not chosen as the type since the abdomen and the hind legs have been broken off. The spurs of the middle and hind tibiae are approximately equal in size and shape. The hind femora are clavate, attenuated on their basal halves. The hind basitarsi are straight-sided, not noticeably thickened, and nearly two times longer than the second tarsal segment. Wings : Entirely dark colored, black along the anterior margin, smoky black over most of the membrane. The base of Rs is slightly longer than the r-m crossvein. The m crossvein is situated about its own length from the forking of veins Ml and M2. Veins M2 and M3+4 evanesce just before the wing margin (Text-fig. 40). Abdomen : Entirely subshining black, densely black pilose. The claspers are slender, rather sharp pointed, the ninth sternum is cleft about half its length and a 20 D. ELMO HARDY pair of small submedian bumps are present on the hindmargin. The basal half of the sternum is semi-membranous down the median portion (Text-fig. 44). The ninth tergum is shaped as in Text-fig. 43, a small mound is present in the middle of the hind margin. Length : Body, 8-9 mm. ; wings, 9-3 mm. ? unknown. Holotype <$, NEPAL : Taplejung Distr., damp evergreen oak forest above Sangu, c. 9,200', 2-26. xi. 1961 (R. L. Coe). One paratype <$, same data as type. Type in the British Museum (Natural History), paratype in the University of Hawaii collection. Genus DILOPHUS Meigen Philia Meigen, 1800, Nouv. Class. Mouches : 20. [A rejected name.] Dilophus Meigen, 1803, Illiger's Mag. 1 (2) : 269. Members of this genus are characterized by having two or three sets of strong spines on each front tibia (Text-fig. 46) and by the simple radial sector of the wing with the basal section of Rs short compared to the r-m crossvein (Text-fig. 50) . The genus has not previously been reported from Nepal, two species are now known to occur there. Type species : Tipula febrilis Linnaeus. Dilophus gratiosus Bigot (Text-figs. 45-47) Dilophus gratiosus Bigot, 1890, /. Asiat. Soc. Beng. 59 : 265. This is the only species of Dilophus which has previously been recorded from the Himalaya region. Brunetti recorded it from several localities in northern India and Upper Burma (1911 : 280 and 1912 : 178). It has been differentiated by the pre- dominantly black body and legs of the male, the predominantly red thorax of the female, the short rostrum and the presence of yellow pile over the body and legs. Two $ specimens on hand appear to be typical gratiosus ; they were not associated with the male and may possibly be the females of the new species hirsutus ; on the basis of the wing and leg characters, however, this seems unlikely. The following descriptive notes are based upon two females from NEPAL, and one <$ from INDIA : Chhatoru, Spiti Valley, 11,000', i6.vi.i955 (A. P. Kapur). o*. Entirely shining black, the body and legs are pale yellow pilose except for dark pile on the tarsi. The thorax is sparsely pilose, with short yellow hairs. Brunetti in his redescription (1912 : 178) said that the posterior margin of the scutellum and the sides of the metapleura are bright brownish yellow, on the specimen at hand there is only a rather faint indication of yellow to rufous in the ground colour of the sides of the scutellum. The rostrum is not produced beyond the bases of the antennae and the sclerotized portion of the head in front of the eyes, measured at the antennal bases, is approximately equal in length to the first two flagellar segments of the antenna. On the specimen at hand the legs are entirely shining black, the claws are brownish red. Brunetti described the legs as reddish brown. The front tibia has a transverse row of four short spines arranged at the middle of the segment (Text-fig. 46). The leg segments are rather slender, the hind basitarsi are about half as long as the tibiae. The wings are subhyaline, faintly yellowish along the costal margin ; the stigma is pale brown. The base of the radial DIPTERA FROM NEPAL sector is approximately one-half as long as the r-m crossvein (Text-fig. 47). The $ genitalia have not been dissected for study. The $ head is polished black, smooth, the front is approximately equal in width to one compound eye. The head is slightly longer than wide, as seen from lateral view it is as in Text-fig. 45. The thorax is predominantly rufous, typically with a dark brown to black vitta extending down the anteromedian portion. The coxae, trochanters, and the first two pairs of 46 .6 mm. £ E CD 47 I. 0 mm. FIGS. 45-47. Dilophus gratiosus Bigot. Fig. 45, head of $ ; Fig. 46, front tibia ; Fig. 47, middle portion of wing. femora are yellow to rufous. Each middle femur is tinged with brown at the apex. The hind femur is yellow to rufous on the basal two-thirds, shining brown to black on the apex. The tibiae and tarsi are shining black. The tibial spines are slightly larger, more prominent than in the (J. The wings are yellow fumose, darker along the costal margin. The stigma and anterior veins are dark brown, the posterior veins are yellow, tinged with brown. The venation is similar to that of the £. The abdomen is brown to black on the dorsum, rufous, faintly tinged with brown on the venter. The cerci are dark brown. Length : Body and wings, 3'5-3'75 mm. Type locality : Dharamsala, western Himalayas. Type in the Indian Museum. The two $ specimens on hand are from NEPAL : Ghanpokhara, 5,500-7,000', 2. v. 1954 (/. Quintan). 22 D. ELMO HARDY Dilophus hirsutus n. sp. (Text-figs. 48-51) This species is somewhat similar to gratiosus Bigot but differs by having the basal section of the radial sector very short, approximately one-fifth as long as the r-m crossvein, rather than being approximately one-half as long as the r-m ; by having the body and legs densely black pilose, rather than sparsely pale pilose ; by having spines at the middle of the front tibia differently arranged as in Text-figs. 49 and 46 ; and the hind basitarsus comparatively short (Text-fig. 48). Also the wings of the male are distinctly fumose and the costal vein extends about half the distance between the apices of the Rs and Mx (Text-fig. 50). cJ. Entirely shining black species, including the appendages, and densely covered with black pile. Head : The eyes are densely covered with moderately long black pile, the hairs are approximately two times longer than the height of the ocellar triangle. The head beyond the eyes is very short, completely obscured by the dense black pile of the front of the head. The palpi are very short and inconspicuous, only two or three short segments are visible on the specimens at hand and the labellum is not extended. The flagellum of the antenna is made up of six to seven segments, the apical segments are closely fused and the apical portion is distinctly enlarged, clavate. Thorax : Predominantly polished black, finely rugose down the median . 2 5 mm. FIGS. 48-51. Dilophus hirsutus n. sp. Fig. 48, hind leg ; Fig. 49, front tibia ; Fig. 50, wing ; Fig. 51, <$ genitalia, ventral. DIPTERA FROM NEPAL 23 portion and on the sides of the mesonotum, also on the pleura and the scutellum. The meso- notum has an abundance of long black hairs on the sides and down the dorsocentral lines. The scutellum is densely black haired around the margin. The pile of the pleura is dark brown to black. The halteres are brown, tinged with yellow on the stems. Legs : Polished black, densely black pilose except for a few scattered yellow ventral hairs on the apical one-half to three-fifths of the hind femur. Four dorsal spines are arranged near the middle of the front tibia ; these are arranged as in Text-fig. 49. The apical spur is equal in size to the apical spines. The hind basitarsus is slender, but rather short, scarcely over one-fourth as long as the tibia (Text-fig. 48). Wings : Faintly infuscated, the anterior veins and stigma are dark brown, the posterior veins are yellow, tinged with brown. The base of the radial sector is approximately one-fifth as long as the r-m cross vein and the fork of veins Ml and Mz is well beyond the m crossvein (Text-fig. 50). The costa extends approximately one-half the distance between the apices of the radial sector and vein Mv Abdomen : Shining black, rather slender, covered with black pile on the basal four segments and yellow pilose on the apical four segments and on the genitalia. The genitalia as seen from ventral view are as in Text-fig. 51, the cleft on the postero- median margin of the ninth sternum is rather shallow and the claspers are rounded, blunt at apices. The ninth tergum is damaged on the specimen which has been relaxed for study. It appears to be about one-half wider than long with a gentle concavity on the posterior margin. Length : Body, 3-5 mm. ; wings, 4-0 mm. $ unknown. Holotype <£ and eight paratypes <$, E. NEPAL : S. of Makalu, 5.ix.i954, 13,500' (L. W. Swan). Type and four paratypes in the California Academy of Sciences, two paratypes are being deposited in the British Museum (Natural History), and two in the collection of the University of Hawaii. REFERENCES BRUNETTI, E. 1911. New Oriental Nematocera. Rec. Indian Mus. 4 : 269-281. - 1912. Fauna of British India including Ceylon and Burma. Diptera Nematocera. Taylor and Francis, London. 581 pp. 12 pis. - 1925. Notes on Oriental Bibionidae with descriptions of new species. Rec. Indian Mus. 27 : 443-450- HARDY, D. E. 1953. Studies on Oriental Bibionidae : New species of Plecia and Penthetna and a revision of the Plecia impostor complex (Bibionidae : Diptera). Rec. Indian Mus. 50 (i) : 89-104. - 1956. The Walker types of Bibionidae (Diptera). /. Kans. ent. Soc. 29 (3) : 85-91. - 1958. The Plecia of the Pacific and Southeast Asia (Bibionidae-Diptera). Pacif. Sci. 12 (3) : 185-220. HARDY, D. E. and M. TAKAHASHI. 1960. Revision of the Japanese Bibionidae (Diptera, Nematocera). Pacif. Ins. 2 (4) : 383-449. DIPTERA FROM NEPAL AGROMYZIDAE By K. A. SPENCER SYNOPSIS This paper is based on 34 specimens collected by R. L. Coe during the 1961-62 British Museum Expedition to East Nepal. Eight species are represented. Two of these are described below as new, one being placed in a new genus, Lemurimyza ; five were previously known from the Oriental region and one, Phytoliriomyza australensis Spencer, has previously only been recorded in Australia and Tahiti. REFERENCES not included will be found in full in my synopsis of Oriental species (Spencer, 1961). Genus JAPANAGROMYZA Sasakawa Japanagromyza trispina (Thomson) comb. nov. Agromyza trispina Thomson, 1869. Agrontyza variihalterata Malloch, 1914. syn. nov. Japanagromyza variihalterata (Malloch) Spencer, 1960 : 17. Taplejung Dist., Sangu, c. 6,200', i $, ix-x.ig6i. I have recently examined the holotype of Agromyza trispina in the Naturhistoriska Riksmuseum, Stockholm. This is a female in good condition which is clearly identical with the widespread Oriental species, /. variihalterata (Malloch) ; varii- halterata is therefore synonymized with trispina herewith. The type locality of trispina is given as " China ", and is presumably somewhere on the southern seaboard ; /. variihalterata was described from Formosa. Genus MELAN AGROMYZA Hendel Melanagromyza metallica (Thomson) Agromyza metallica Thomson, 1869. Melanagromyza metallica (Thomson) Spencer, 1959. Arun Valley, Tumlingtar, East shore of Riv. Arun below Tumlingtar, 1,800', i<$, 2 £, 14-23. xii. 1961. Taplejung Dist., Dobhan, c. 3,500', Riv. Maewa, i<$, 2.1.1962 ; Sangu, c. 6,200', i $, 16-29. x. 1961 '• I ?» ix-x.i96i. The biology of this widespread species has recently been clarified. In November 1962 I found larvae in stems of Ageratum conyzoides L. at Delhi but failed to breed any adults ; in January 1963 V. K. Sehgal, who was collecting with me at Delhi, found some more larvae in the same host (India : Bihar, Namkum, Ranchi,) and the adults sent to me for examination proved to be metallica. Sehgal has subse- quently bred the species also from Bidens pilosa L. and it no doubt also occurs in other Compositae. Bull. Brit. Mus. (Nat. Hist.), Ent. 16 (i), 1965. 26 K. A. SPENCER Melanagromyza phaseoli (Tryon) Oscinis phaseoli (Tryon) Spencer, 1895. Melanagromyza phaseoli (Tryon) Spencer, 1959. Taplejung Dist., between Sangu and Tamrang, c. 5,500', i $, 23.x. 1961. Genus CERODONTHA Rondani Nowakowski (1962) has recently transferred the sub-genus Icteromyza from Phytobia to Cerodontha and I here follow this new classification. Cerodontha (Icteromyza) duplicata (Spencer), comb. nov. Phytobia (Icteromyza) duplicata Spencer, 1961. Taplejung Dist., between Sangu and Tamrang, shrubs by path, c. 5,800', i <£, i $, 6.xi.T_96i ; dense vegetation in tree shade by hill stream, 3 <£, 3 $, 23.x. 1961 ; Sangu, c. 6,200', mixed vegetation by stream in gully, 2 $, I $, ix-x.i96i and xi. 1961-1.1962 ; on yellow blooms of cultivated Composite, 2 <£, 16-29. x. 1961 '> below Sangu, c. 4,000', mixed vegetation on sheltered slopes above river, i <$, 2 $, 3.1.1962 ; river banks below Tamrang bridge, c. 5,500', i <£, x-xi.i96i ; edge of mixed forest above Sangu, c. 6,500', 3 $, I7.x.-i.xi.i96i. This series represents the second record of this species which was described from a single male from INDONESIA : Flores. Genus LIRIOMYZA Mik Liriomyza compositella Spencer Liriomyza compositella Spencer, 1961. This leaf -miner on Compositae is widespread in the Oriental Region. In November 1962 I bred a long series from leaf-mines on Xanthium strumarium L. at Delhi. LEMURIMYZA gen. n. (Lemuria and myza) (Text-figs. 52-58) Frons broad, one and a quarter to twice width of eye, two upper fronto-orbital bristles, one lower ; orbital setulae minute, proclinate, upright, reclinate or lacking ; acrostichals sparse, in only two rows ; small species, wing length 1-75 to 2-3 mm. ; sub-costa reaching costa inde- pendently of vein rlt costa extending to vein M1+2, second crossvein present. Colour : head largely yellow, third antennal segment yellow or black ; mesonotum black but with yellow patch in centre before scutellum ; scutellum yellow, at least centrally ; halteres black or yellow. ^ GENITALIA : distiphallus in form of characteristic paired tubules (Text-figs. 53, 56, 58), mesophallus dark, cylindrical, surstyli separated by wide suture from ninth tergite, bare or with a few hairs and/or spines, linked to basal end of ninth tergite by strong, black, comb-like process (Text-figs. 54, 57, 59) ; ninth sternite with narrow side-arms, somewhat elongated ; spermal sac either minute (as in enormis, Spencer, 19636 : fig. ic and dorsata) or more normal (as in admirabilis, fig. 55). DIPTERA FROM NEPAL 27 Type species : Liriomyza enormis Spencer, 19636 : 114 by present designation. This genus appears to occupy an intermediate position between Liriomyza Mik and Phytoliriomyza Hendel. The orbital setulae are intermediate between the distinctly reclinate setulae of Liriomyza and the distinctly proclinate setulae of Phytoliriomyza. The form of aedeagus approaches that found in some species of Phytoliriomyza, such as P. lurida Spencer from Brazil (Spencer, 19630 : 379). In many species of Phytoliriomyza the halteres are partially darkened. The shape of the head is more typical of Liriomyza. The genus Lemurimyza can be included in the author's (1961 : 57) key to Oriental genera by amending and extending couplet 8 as follows : second alternative, for Liriomyza Mik read SA ; add new couplet : 8 A Halteres dark brown ; if yellow, orbital setulae incurved, sparse or lacking Lemurimyza Spencer — Halteres yellow ; orbital setulae distinctly reclinate . . Liriomyza Mik 54 55 FIGS. 52-55. Lemurimyza admirabilis sp. n. : Fig. 52, head ; Fig. 53, aedeagus and ninth sternite, ventral view ; Fig. 54, surstylus ; Fig. 55, spermal sac. (Scale line represents o-i mm. for genitalia drawings). 28 K. A. SPENCER Four species can immediately be grouped into this genus : Liriomyza enormis Spencer from Madagascar ; L. admirabilis sp. n. from Nepal described below ; and Agromyza dorsata Siebke and A. pectoralis Becker from Europe. These four species can be identified by the following key : 1 Halteres dark, brownish-black . . . . . ... . . 2 — Halteres pale, yellow ........... 3 2 Third antennal segment yellow ....... enormis (Spencer) — Third antennal segment black ...... admirabilis sp. n. 3 Palps yellow . . . . . . . . . dorsata (Siebke) — Palps black .......... pectoralis (Becker) Lemurimyza enormis (Spencer) comb. nov. Liriomyza enormis Spencer, 19636. Holotype <$ in Musee d'Histoire Naturelle, Paris. This species was originally placed in Liriomyza with some hesitation in view of its dark halteres and aberrant genitalia. With the discovery of a further closely related species in Nepal, with the same essential characters, the erection of a new genus is clearly justified. Lemurimyza admirabilis s.p. n. (Text-figs. 52-55) Head (Text-fig. 52) : frons broad, twice width of eye viewed from above, not projecting above eye in profile ; two equal, reclinate ors, one slightly weaker, incurved ori ; orbital setulae minute, sparse, upright ; third antennal segment rounded, arista long, appearing bare. Mesonotum : 3 + 1 dorso-centrals, acrostichals sparse, in two rows at front, not extending behind third dc. Wing : length in male 1-75 mm., costa extending strongly to vein m1+2, discal cell large with vein rm at midpoint, last section of vein ws+4 not greatly longer than penultimate, in ratio 18 : 13. Colour : frons and jowls orange yellow, lunule paler, more lemon yellow ; face yellowish- grey ; third antennal segment black, second dark, blackish but distinctly paler with a trace of yellow, third yellow ; mesonotum matt black, with a small oval area adjoining scutellum yellow, not extending to level of first dorso-central ; scutellum yellow centrally, gradually becoming grey laterally ; notopleural area yellow, mesopleura yellow above, black below (exact colour not detectable, owing to damage to specimen) ; sternopleura black below with broad yellow upper margin ; legs appearing entirely black but fore-femora somewhat yellow on inside ; abdomen entirely black ; squamal fringe black ; halteres black. c? GENITALIA : aedeagus as in Text-fig. 53 ; distiphallus with paired terminal processes, mesophallus dark, blackish, cylindrical, distinctly broader at base, equal in length to distiphallus ; hypophallus in form of two narrow, somewhat irregular ventral appendages arising from base of mesophallus ; ninth sternite with narrow side-arms, elongate (Text-fig. 53) ; surstyli (Text- fig. 54) a black, comb-like process adjoining ninth tergite, then broadening apically into a large flat plate ; spermal sac with rather broad blade, stalk narrow (Text-fig. 55). Holotype <$, NEPAL : Taplejung Distr., river banks below Tamrang bridge, c. 5,500' x.-xi., 1961 (R. L. Coe), in British Museum (Nat. Hist.). Lemurimyza dorsata (Siebke) comb. nov. Agromyza dorsata Siebke, 1864. Holotype $ in Zoologisk Museum, Oslo. Liriomyza striata Hendel, 1931-6 : 249. syn. nov. Holotype 9 in Naturhistorisches Museum, Vienna. DIPTERA FROM NEPAL Material examined : AUSTRIA : Vienna, meadows beside Danube, i $, 5.vi. (Hendel), holotype of striata. CZECHOSLOVAKIA : Tatra, i <$, genitalia slide 925, (Kertesz). ENGLAND : Staffs., Madeley, i £, genitalia slide 880, 25.vii. FIGS. 56-61. Lemurimyza dorsata (Siebke) : Fig. 56, aedeagus, ventral view ; Fig. 57, surstylus ; Lemurimyza pectoralis (Becker) : Fig. 58, aedeagus, ventral view ; Fig. 59, surstylus. Phytomyza nepalensis sp. n. : Fig. 60, head ; Fig. 61, wing. (Scale line represents o-i mm.). 3o K. A. SPENCER 1926 (H. Britten). FINLAND : Helsinki, i $, genitalia slide 927, no date (R. Frey). NORWAY : Jerkin, i <$ (abdomen missing), 27^11.1853, holotype of dorsata ; Fjell- froskvann, i <$, 23.vii.i926 (Ryden, 1957). The distinctive aedeagus and surstyli of this species are shown in Text-figs. 5, 6. Hendel (1931-6 : 203) incorrectly synonymized Agromyza dorsata with Phytolirio- myza perpusilla Meigen. Ryden (1955) similarly synonymized A. dorsata with Phytoliriomyza halterata Becker, which at that time was thought to be identical with perpusilla. This confusion arose understandably from the similarity of these species on external characters. Clarification has only been possible with recent study of the male genitalia. Lemurimyza pectoralis (Becker) comb. nov. Agromyza pectoralis Becker, 1908 : 167. Holotype $ in Zoologisches Museum, Berlin. Liriomyza pectoralis (Becker) Hendel, 1920 : 144 ; 1931-6 : 241. I have examined the holotype from the CANARY ISLANDS : Tenerife and the characteristic aedeagus and surstyli are shown in Text-figs. 58, 59. This species is widespread but local in the Mediterranean area. I caught a series of 12 specimens on the lower slopes of Mt. Etna, Sicily on 8-9.^.1964. Genus PHYTOLIRIOMYZA Hendel Phytoliriomyza australensis Spencer Phytoliriomyza australensis Spencer, I9&3A : 335. Phytoliriomyza tahitiensis Sasakawa, 1963. syn. nov. [from description and figures]. Arun Valley, East shore of R. Arun below Tumlingtar, c. 1,800', swept from Ricinus communis L., i $, 23.xii.i96i. Taplejung Dist., Sangu, c. 6,200', mixed vegetation by stream in gully, 2 J, xi. 1961^.1962. This species was previously only known from various localities in New South Wales. Genus PHYTOMYZA Fallen Phytornyza nepalensis sp. n. (Text figs. 60-6 1 ) Head (Text-fig. 60) : frons exceptionally broad, slightly over twice width of eye at foremost ocellus, not significantly projecting above eye in profile ; orbits unusually broad, well-differen- tiated, two equal, reclinate upper orbital bristles, one similar incurved lower orbital ; eye upright, oval, jowls deepest in centre, one-quarter vertical height of eye, cheeks well-developed below eye ; third antennal segment almost round, arista short. Mesonotum : acrostichals irregularly in two rows at front, not extending to second dorso- central ; inner post-alar strong, similar to fourth dc. Wing (Text-fig. 61) : length 2-1 mm., costal ratio 30 : 12 : 16, second section just less than twice length of fourth. Colour : an entirely black species ; orbits, mesonotum and abdomen brilliantly shining. DIPTERA FROM NEPAL 31 Holotype $, Nepal, Taplejung Distr., c. 6,500', edge of mixed forest above Sangu, I7.x.-i.xi.i96i (R. L. Coe), in the British Museum (Natural History). This species somewhat resembles Phytomyza hendeli Hering (cf. Hendel, 1931-6 : 413), a leaf -miner on Anemone in Europe but is obviously distinct, in view of its darker head, more shining mesonotum and sparser acrostichals. No comparable black species is known from Japan, nor from the Oriental and Australian regions. REFERENCES BECKER, TH. 1908. Dipteren der Kanarischen Inseln. Mitt. zool. Mus. Berl. 4 : 1-180. HENDEL, F. 1920. Die palaarktischen Agromy ziden (Dipt.). A rchiv.Naturgesch. 84 : 111-175. - 1931-6. Agromyzidae in Lindner. Flieg. pal. Reg. 59 : 1-570. NOWAKOWSKI, J. T. 1962. Introduction to a Systematic Revision of the Family Agromyzidae (Diptera). Ann. zool. Warsaw. 20 : 67-183. RYDEN, N. 1955. Norska Agromyzider. Norsk ent. Tidssk. 9 : 230-234. - 1957. Norwegische Agromyziden. 2. Astarte 14 : 1-4. SASAKAWA, M. 1963. A Revision of the Polynesian Agromyzidae. Pacif. Insects 5 : 489-506. SIEBKE, H. 1864. Beretning om en i Sommeren 1861 foretagen entomologisk Reise. Nyt. Mag. Naturv. 12 : 169. SPENCER, K. A. 1959. A Synopsis of the Ethiopian Agromyzidae. Trans R. ent. Soc. Land. Ill : 237-329. - 1960. Records of further Ethiopian Agromyzidae. ibid. 112 : 15-36. - 1961. A synopsis of the Oriental Agromyzidae. ibid. 113 : 55-100. - 1962. Notes on the Oriental Agromyzidae — i. Pacif. Insects 4 : 661-680. - I963A. The Australian Agromyzidae. Rec. Aust. Mus. 25 : 305-354. - 19636. Notes on the Agromyzidae of Madagascar — i. Proc. R. ent. Soc. Lond. (B) 32 : 114-116. - I963C. A synopsis of the neotropical Agromyzidae. Trans. R. ent. Soc. Lond. 115 : 291- 389- PRINTED IN GREAT BRITAIN BY THOMAS DE LA RUE & COMPANY LIMITED LONDON ', /& AUG1965 A SYSTEMATIC REVISION OF Tl" AMENIINAE (DIPTERA: CALLIPHORIDAE) R. W. CROSSKEY BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ENTOMOLOGY Vol. 16 No. 2 LONDON : 1965 A SYSTEMATIC REVISION OF THE AMENIINAE (DIPTERA : CALLIPHORIDAE) BY R. W. CROSSKEY Yvj Commonwealth Institute of Entomology, ^London Pp. 33-140 ; 50 Text-figures BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY) ENTOMOLOGY Vol. 16 No. 2 LONDON: 1965 THE BULLETIN OF THE BRITISH MUSEUM (NATURAL HISTORY), instituted in 1949, is issued in five series corresponding to the Departments of the Museum, and an Historical Series. Parts will appear at irregular intervals as they become ready. Volumes will contain about three or four hundred pages, and will not necessarily be completed within one calendar year. In 1965 a separate supplementary series of longer papers was instituted, numbered serially for each department. This paper is Vol. 16, No. 2 of the Entomology series. The abbreviated titles of periodicals cited follow those of the World List of Scientific Periodicals. Trustees of the British Museum (Natural History) 1965 Price £i 155. A SYSTEMATIC REVISION OF THE AMENIINAE (DIPTERA : CALLIPHORIDAE) By R. W. CROSSKEY CONTENTS Page SYNOPSIS ........... 36 INTRODUCTION ........... 36 MATERIAL STUDIED .......... 37 METHODS EMPLOYED. ......... 37 Taxonomic characters, terms and measurements .... 37 Abbreviations .......... 40 RELATIONSHIPS AND SYSTEMATIC STATUS OF THE GROUP . . . 41 SUBFAMILY AMENIINAE ......... 45 Diagnosis and bibliography ........ 45 Key to the tribes of Ameniinae ....... 46 Systematic treatment ......... 46 TRIBE AMENIINI Brauer and Bergenstamm .... 46 Key to the genera of Ameniini ...... 47 Silbomyia Macquart ......... 50 Key to the species ........ 53 Descriptions of the species ....... 56 Platytropesa Macquart ........ 84 Key to the species ........ 85 Descriptions of the species ....... 85 Stilbomyella Malloch ......... 93 Key to the species ........ 95 Descriptions of the species ....... 95 Paraplatytropesa gen. n. ........ 98 Description of the species ....... 99 Amenia Robineau-Desvoidy . . . . . . . 100 Key to the species ........ 104 Descriptions of the species . . . . . . . 105 Formosiomima Enderlein . . . . . . . . 122 Description of the species . . . . . . . 124 TRIBE PARAMENIINI Enderlein 125 Paramenia Brauer and Bergenstamm . . . . . . 126 Key to the species ........ 127 Descriptions of the species . . . . . . . 128 SUMMARY OF REVISED CLASSIFICATION OF AMENIINE FLIES . . . 137 ACKNOWLEDGMENTS . . . 138 REFERENCES ........... 139 36 R. W. CROSSKEY SYNOPSIS The Ameniinae are fully revised and their affinities discussed ; no evidence is found of affinity with true Tachinidae, and contrary to usual practice the group is excluded from this family and treated as a subfamily of Calliphoridae. Seven genera (one new) and thirty-one species (nine new) are recognised ; five generic, eleven specific and one subspecific name are newly placed in synonymy, and there are five new generic combinations. Keys are provided for the identifica- tion of all genera and species, and a summary is given of the revised classification proposed. INTRODUCTION A GENERAL systematic study of the Tachinidae of the Oriental and Australian regions currently in progress has necessitated a study of the Ameniine flies to determine whether the group should, following the majority of authors, be included in the true Tachinidae or whether its affinities lie with the Calliphoridae. Townsend (1935, 1937) and van Emden (1950, 1951), departing from earlier work, placed the group in the Calliphoridae, but Paramonov (1957) has more recently treated the Ameniine flies as a tribe of Tachinidae allied to the Rutiliini ; in the present work the group is treated, on the basis of evidence adduced in a later section, as a sub- family of Calliphoridae. The Ameniinae is certainly an anomalous group, and has been much neglected by specialists on higher Diptera ; apart from the scattered papers of Malloch (1927, igaSa, igaSb, 1929, 1930, 1933, 1935) only the revisions of Rutiliinae by Engel (1925) and Enderlein (1936), and a review of Australian species by Paramonov (1957), have been available for identification. Unfortunately neither Engel nor Enderlein saw the types of most of the species they discussed, and both saw very little material, so that their work is much confused by mis- identification, and most of the names in Hardy's (1938) key to the species of Amenia are also misapplied. To unravel past confusion it has been necessary here to give a full re-description of all species, especially since several species were hitherto known only from a few brief lines in old scattered works of nineteenth-century authors. Thirty-seven previously described species are involved in this revision and the holotypes or syntypes of thirty-five of these have been examined, thirty-two personally and three (the types were not available on loan) by specialist colleagues. Paratypes of one other species have been examined which are undoubtedly con- specific with the holotype, and the type of the one remaining species is lost (Amenia imperialis Robineau-Desvoidy, for which a neotype is designated on page 109). A lectotype has been designated and labelled for each species without specified holotype and based on syntypes, and the available syntypes left after lectotype designation have each been labelled as paralectotype. After examination of types only twenty-two of the thirty-seven previously described species are upheld in the present work, giving, with the nine new species, a total fauna of thirty-one species in the Ameniinae ; two of the previously described species (Ptylostylum albomaculatum Macquart and Amenia dubitalis Malloch) are accorded subspecific status only. The remaining thirteen names of previously REVISION OF THE AMENIINAE 37 described species are here treated in synonymy, eleven being newly established synonyms ; the one previously published subspecific name (enderleini Paramonov, see p. 115) is also synonymized. Of the fourteen described genera belonging in the Ameniinae only six are regarded as valid ; one new genus is added. MATERIAL STUDIED No single institution has an extensive collection of Ameniine flies, and the present work is based on a study of 746 specimens assembled from the following museums (abbreviations given are those used throughout the text in the lists of material examined) : British Museum (Natural History), London (B.M. Nat. Hist.) ; Deutsches Entomologisches Institut, Berlin (D. Ent. Inst.) ; Division of Entomology Museum, C.S.I.R.O., Canberra (Div. Ent. Mus. Canberra) ; Naturhistorisches Museum, Vienna (Nat. Mus. Vienna) ; Rijksmuseum van Natuurlijke Historic, Leiden (Rijksmus. Leiden) ; School of Public Health and Tropical Medicine, Sydney (S.P.H.T.M.) ; Staatliches Museum fur Naturkunde, Stuttgart (Staatl. Mus. Stuttgart) ; United States National Museum, Washington (U.S. Nat. Mus.) ; Universitetets Zoologiske Museum, Copenhagen ; University Museum, Oxford (Oxford Mus.) ; Zoologisch Museum, Amsterdam (Zool. Mus. Amsterdam) ; Zoologische Sammlung des Bayerischen Staates, Munich (Zool. Sammlung, Munich) ; Zoologisches Museum der Humboldt-Universitat, Berlin (Zool. Mus. Humb. Univ.). METHODS EMPLOYED Taxonomic characters, terms and measurements At present only adult morphological characters are available for classification. In many Calyptrate flies the male genitalia are of great value in providing specific characters, but in the Ameniinae the male hypopygium is extremely uniform morphologically (cf. Text-figs. 31-42) and is usually virtually indistinguishable even in forms belonging in different genera and differing enormously on external charac- ters. Only in a few species do the male genitalia provide valuable systematic characters, and classification of the Ameniinae must at present be based almost entirely on non-genitalic characters. The head provides the most useful characters : terms used for head regions and chaetotaxy are shown in Text-figs, i and 2, and the measurement points used in determining the relative proportions of different head structures are shown in Text-figs. 3-6. The following structural proportions often provide valuable specific characters : length of facial carina (D) relative to epistome (E) or distance from lunula to anterior ocellus (A) ; width of interfrontal area (B) relative to width of parafrontal at corresponding point (C) (measured at level of lower proclinate orbital INTERFRONTAL AREA R. W. CROSSKEY PROCLINATE ORBITAL SETAE PREVERTICAL SETA PARAFRONTAL INNER VERTICAL SETA PARAFACIAL FACIAL RIDGE EPISTOME POSTBUCCA I 2 FIGS, i and 2. Head of an Ameniine fly showing terms used in text. Drawn from Silbomyia latigena Enderlein. seta since this provides fixed landmark) ; length of third antennal segment relative to second (F to G) ; width of parafacial (H) at mid point relative to width of third antennal segment (J) ; width of gena (K) as proportion of eye-height (L) ; width of vertex (N) relative to one eye viewed from above (M) in females and males with broad frons ; width of frons at narrowest point (P) as proportion of head width (Q) in males with approximated eyes. Measurements A, B, C, H, and J have been made with the head appropriately oriented so as to avoid foreshortening effect of straight facial or profile view. Head chaetotaxy is of little or no value at specific level, but presence or absence of outer vertical, prevertical and proclinate orbital setae in males is of some value as a supporting generic character. Thoracic chaetotaxy is very uniform and provides no useful characters except that the position of the outer posthumeral seta (whether mesad or laterad of a longitudinal line through the presutural seta — Text-figs. 9 and 10) is a secondary, character supporting the distinction of two tribes ; however even this character must be used with caution, since the outer posthumeral seta may be missing altogether in some specimens. Similarly the presutural intra-alar seta may be present or absent, but systematic importance cannot be attributed to this ; certain setae may in freak specimens be duplicated (giving for instance five instead of the normal four postsutural dorsocentral setae, or four instead of the normal three sternopleural setae). The chaetotaxy of the legs is also uniform, but the presence REVISION OF THE AMENIINAE 39 FIGS. 3—6. Outline drawings of head of Ameniine fly showing measurement points used for determining proportions of head structures. Lunula to anterior ocellus (A). Width of interfrontal area (B) relative to parafrontal at level of lower proclinate orbital seta (c). Length of facial carina (D) relative to epistome (E). Length of third antennal segment (F) relative to second segment (G). Width of parafacial at mid point (H) relative to width of third antennal segment (j). Width of gena (K) as proportion of eye-height (L) . Width of vertex (N) relative to one eye viewed from above (M) in females and males with broad frons. Frons width at narrowest (P) as proportion of total head width (Q) in males with reduced frons and strongly approximated eyes. or absence of postero-dorsal setae on the fore tibia and the number (whether one or two) of postero-ventral setae on this tibia are of some generic value ; the number of antero-dorsal setae on the mid tibia usually varies within a species, but is of some value as a specific character in Paramenia. 40 R. W. CROSSKEY In the wings the degree of infuscation is remarkably constant within a species and differs between species, providing a useful character in Silbomyia. Wing venation varies only in detail, in the forward bowing of the costa of the males of some Amenia, in the remoteness of the bend of vein M from the wing margin and the position of r-m cross-vein relative to the discal cell. Where appropriate, measurements have been made of the relative proportions (see Text-fig. 17) of r-m to m-cu, m-cu to bend of M, and bend to wing-margin (point of measurement on the wing margin determined by where an imaginary line extended from M basad of the bend intersects with the margin). A previously undiscovered character of great use in denning Silbomyia is the presence of fine setulae on the ventral surface of the second costal sector (Text-fig. 23). Abdominal chaetotaxy is of very limited use : presence or absence of median marginal setae on Ti + 2 is of some value in Silbomyia, and the unusual character of an irregular row of marginal setae on T4 is diagnostic for Formosiomima. The inclination (whether erect or recumbent) of hair on the tergites and the presence of long dense hair on the venter of some males also provide characters. Abdominal shape differs but provides a character difficult to define satisfactorily. The fifth sternite of the <$ produces no bizarre developments such as occur in many Calyptrates and is of almost no taxonomic value in Ameniinae, except to a limited extent in Platytropesa. The arrangement of white pollinosity on thorax and abdomen is very constant within the species and often provides a dependable character ; colour of head pollinosity and the underlying ground colour are also important. Thoracic and abdominal colour vary in most species from green to violaceous, but colour provides a useful character in Amenia and Paramenia where there is greater constancy. Body length has been measured from the leading edge of facial carina to the apex of the abdomen with fly viewed in profile, and the wing length measured from the base of the epaulet. Abbreviations The abbreviations used in the keys and descriptions are as follows : Thoracic setae : acr, acrostichal setae ; dc, dorsocentral setae ; ph, outer posthumeral seta ; prs, presutural seta ; prst dc, presutural dorsocentral setae ; prst ia, presutural intra-alar setae. In describing the positions of setae on the legs the convention is followed of imagining the leg to be extended at right-angles to the longitudinal axis of the fly, when : a, anterior ; ad, antero-dorsal ; pd, postero-dorsal ; pv, postero-ventral. Wings : m-cu, posterior cross-vein ; M, fourth vein ; R±, first vein ; Rz+3, second vein ; -R4+5, third vein ; Sc, subcosta. Abdomen : T=tergite ; the composite first apparent tergite is Ti+2, and successive tergites are numbered accordingly, the last apparent tergite therefore T5 (as in Text-fig. 27). REVISION OF THE AMENIINAE 41 RELATIONSHIPS AND SYSTEMATIC STATUS OF THE GROUP Amenta and its allied genera were fiist given family-group status by Brauer and Bergenstamm (1889), who erected the Ameniidae as " Gruppe XLVI " in their classification of the " Muscaria Schizometopa ". Although given a family ending the " Gruppen " of Brauer and Bergenstamm are approximately equivalent to tribes in current classifications of Tachinoid Diptera, and no recent author has accorded family status to the group. Brauer and Bergenstamm (1889) placed their Ameniidae immediately before their groups Amphiboliidae (Gruppe XLVII) and Rutiliidae (Gruppe XLVIII), and in their later systematic catalogue (Brauer and Bergenstamm, 1891 : 417-418) sandwiched the group between their Paradexiidae (Gruppe XXV) on the one hand and their Amphiboliidae and Rutiliidae on the other ; such arrange- ment clearly implied that Brauer and Bergenstamm considered the affinities of Amenta and relatives to lie with the Dexillinae and Rutiliinae, groups now forming part of the Tachinidae. It is not surprising that Brauer and Bergenstamm should have reached this conclusion, since the superficial resemblance between Ameniinae and Rutiliini (the large size and metallic coloration and the heavily carinate face of most forms) is very remarkable, but it must now be recognized that the resemblances are convergent and that the affinities of the Ameniinae are almost certainly with the Calliphoridae and not at all with the Tachinidae. It is of interest to note that Robineau-Desvoidy had evidently recognized this in 1830, for in his " Essai sur les Myodaires " he at first (p. 320) placed leonina Fabricius, type-species of Amenta, in Rutilia Robineau- Desvoidy among his " Macropodees " but later in the same work (p. 444) assigned this species to his new genus Amenta near Chrysomya Robineau-Desvoidy in his " Muscides Me"talliques ", remarking that " C'est a tort que j'ai place cette belle espece [leonina] parmi les Macropodees"; in moving leonina from his "Macro- podees " to his " Muscides Metalliques " he was in effect moving it from a group now considered Tachinidae to a group now considered Calliphoridae (Robineau- Desvoidy has been the subject of unjustified obloquy by later dipterists but this example underlines his remarkable eye for affinity). In recent times only Townsend (1935, 1937), van Emden (1950, 1951) and Herting (1957 : 441) have considered the affinities of the Ameniinae to lie with the Calli- phoridae ; Townsend included Amenia and its allies in the Calliphorini, but gave no reasons for this radical departure from their previous position in Tachinidae. Van Emden (1950) drew attention to certain Calliphorid characters in the Ameniini, especially the male hypopygium (Engel, 1925, although placing Silbomyia and Paramenia in Rutiliinae, also noted the resemblance between the male genitalia of these genera and those of Calliphoridae and Hall, 1948 : 7, remarked that inSilbomyia " the form of the male genitalia is conspicuously calliphorid "). The slight develop- ment of a swollen postscutellum in Ameniinae (which led Malloch, 1927, to include the group in the Tachinidae instead of the Calliphoridae) is certainly an unreliable indicator of affinity, for a slightly swollen postscutellum occurs in several undoubted Calliphoridae, and that of the Ameniinae does not in any way resemble the very strongly swollen and smoothly convex postscutellum characteristic of true Tachinidae. 42 R. W. CROSSKEY Other external characters also support Townsend's and van Emden's view of Ameniine affinities : a unique character of all Ameniinae not previously recorded is the characteristic tuft of long black hairs on the anterior lappet of the metathoracic spiracle (Text-fig. 8) ; no such tuft of hairs ever occurs in true Tachinidae, but some Calliphorinae have a few hairs in this position (e.g. Catapicephala Macquart, prs 10 /f pv \f pv II 12 FIGS. 7-12. 7. Ventro-apical view of $ terminalia of Ameniinae in situ, drawn from Amenia sexpunctata Malloch. 8. Metathoracic spiracle in Ameniinae : anterior lappet with characteristic group of long strong hairs. 9. Showing outer posthumeral seta (ph) in Ameniini, lying mesad of presutural seta (prs). 10. Showing outer posthumeral seta (ph) of Parameniini, lying laterad of presutural seta (prs). n. Posterior surface of fore tibia of Platytropesa. 12. Posterior surface of fore tibia of Stilbomyella. REVISION OF THE AMENIINAE 43 which closely resembles the Ameniinae and to some extent interconnects them with the Calliphorinae). The most telling evidence that the Ameniinae are not Tachinidae is provided by what little is known of their biology. Townsend (1942 : 229) recorded that Amenta was parasitic upon the Melolonthid beetles Lepidiota and Lepidoderma and this record was accepted and repeated by van Emden (1950 : 196) but Hardy (1951 : 96) has pointed out that the record is erroneous and derives merely from a supposition in the economic literature given currency by Illingworth (1921 : 42) : the Ameniinae are certainly not parasites of the grubs of these sugar-cane beetles. It is now established from a brief note of Hardy (1951), later amplified by van Emden (1953), that Amenta leonina larvae occur in snails, and these authors assume that the Ameniinae are true parasites of living Mollusca, although this is not fully authen- ticated by evidence so far available. The Ameniinae are undoubtedly larviparous and the female terminalia (Text-fig. 7) are typical of larviparous Calyptrate flies (see Herting, 1957 : 441-443) ; the post- abdomen does not form a telescopic ovipositor as in typical Calliphorinae. There is no doubt that the larvae of Ameniinae are retained in the uterus to a very advanced stage of development (" macrolarviparity "), and it is obvious from the extensive development of soft membrane between the terminal sclerites of the female abdomen that it is modified for the deposition of very large larvae : probably only a single larva develops at one time, as in the South American Mesembrinellinae (Calli- phoridae) and the African Glossinidae. The little-known observation of Illingworth (1921 : 42) supports this and deserves quotation : ' The fourth [species : i.e. Amenta imperialis] is a brilliant green species with a bright yellow face . . . Dissection of the females, however, showed that they still retained a few maggots of rather large size ; and in one instance a maggot about f inch in length was dropped by a fly that I was holding rather tightly ". That the Ameniinae mature the larvae in utero and that the larvae attack snails confirms beyond doubt that the group cannot be included in the Tachinidae, for all true Tachinidae ( from which I exclude the Rhinophoridae parasitic upon terrestrial Isopoda) are endoparasites of other insects in the larval stage and none retain the larvae until nearly mature. Some genera of Sarcophagidae are parasitic in snails, and despite the very great superficial difference (the Ameniinae being large metallic flies) it is possible that the Ameniinae are as closely related to the Sarcophagidae as to the Calliphoridae. When more evidence is available on the biology of the group it may be better to treat it as a full family situated between the Sarcophagidae and the Calliphoridae, but for the present I consider it best to include it within Calliphoridae. Family limits within the Tachinoidea (this superfamily as here used includes the Tachinidae, Rhinophoridae, Sarcophagidae including Miltogrammatinae, and Calliphoridae) are in need of revision, but an improved classification would probably result if the peculiar groups such as Mesembrinellinae were treated as families : this curious group (which despite the presence of hypopleural setae may not be Tachinoidea at all) appears to be a Neotropical analogue to the Australian Ameniinae, also having 44 R- W. CROSSKEY a non-telescopic female postabdomen and depositing mature larvae (Hall, 1948). Zumpt (1956) includes the Sarcophaginae and Miltogrammatinae within the Calliphoridae, and uses the position of the outer posthumeral seta (whether laterad or mesad of the presutural seta) to distinguish these groups from Calliphorinae (Calliphoridae proper) ; this character appears to work for African forms and Palaearctic forms (Mesnil, 1944, uses it as a key character distinguishing Calli- phorinae from Sarcophaginae), but present work casts some doubt on its value when the world fauna is considered. In the Ameniinae the outer posthumeral seta is almost always (tribe Ameniini) situated mesad of the presutural seta, but in Paramenia (Parameniini) is inserted laterad of the presutural seta — so that on Zumpt's (1956) key segregation by means of the outer posthumeral seta the Ameniini would enter the Calliphorinae and the Parameniini would run to the Sarco- phaginae. There is an impressive concordance of characters between Ameniini and Parameniini (here jointly composing the subfamily Ameniinae) and it seems almost certain that the Ameniinae is monophyletic ; if so, then the character of the position of the outer posthumeral seta no longer appears a reliable one for subfamily definition. Another dubious character is that of the presence or absence of minute hairs on the postorbits which Malloch (1935) remarked upon as a character distinguishing most Calliphoridae from most Tachinidae, and which Hall (1948), under the name " intrapostocular cilia " has used to distinguish all Sarcophagidae from most Calliphoridae ; in Ameniine flies the intrapostocular cilia are usually present (another typical Calliphorid character), but are variable and may or may not be present in specimens of the same species. It should be noted that Senior White, Aubertin and Smart (1940) omitted the Oriental genus Silbomyia from their treatment of Oriental Calliphoridae, and presumably considered it as lying outside the limits of this family. However, they included Catapicephala Macquart in their Calliphorinae although this genus shows several features tending towards Ameniinae and away from typical Calli- phorniae (non-telescopic female postabdomen, weakly developed postscutellum, few hairs on anterior lappet of metathoracic spiracle, etc.). No entirely satisfactory characters appear to exist for defining supra-generic taxa in the Calliphoridae (or indeed in any Calyptrate flies) but the Ameniinae as here defined can be distinguished from other subfamilies reasonably easily by the following abbreviated key:* i Metathoracic spiracle with single large reniform lappet with dorsal opening. Vein M with evenly rounded bend. Female postabdomen not forming telescopic ovipositor. [Neotropical Region] .... MESEMBRINELLINAE Metathoracic spiracle with normal anterior and posterior lappets. Vein M with bend distinctly angulate. Female postabdomen usually forming telescopic ovipositor. [All regions] .......... 2 * Sarcophagidae and Rhinophoridae, sometimes treated as Calliphoridae, are here regarded as separate families, and Pollenia and allies (sometimes treated as separate subfamily) are included in Calliphorinae. REVISION OF THE AMENIINAE 45 2 Stem-vein of wing with long fine setulae posteriorly on upper surface. Subalar bulla sometimes setulose .... RHINIINAE and CHRYSOMYIINAE - Stem-vein of wing bare. Subalar bulla always bare ...... 3 3 Anterior lappet of metathoracic spiracle with a conspicuous backwardly-directed tuft of long hairs (Text-fig. 8) . Postscutellum forming a definite convex swelling which is micro-rugose and shows slight trace of shallow median incision. Female postabdomen non-telescopic, modified for deposition of mature larvae. Head almost always with very strong facial carina separating antennae and reaching epistome. [Apparently parasites of living land snails, Oriental and Australian Regions] AMENIINAE - Anterior lappet of metathoracic spiracle bare or at most with a very few small inconspicuous hairs. Postscutellar region not at all convex or at most with rudimentary trace of swelling, not as above. Female postabdomen forming a telescopic ovipositor (some exceptions). Head without a facial carina or at most with rudimentary trace of carina between antennal bases. [Not parasites of snails. All regions] . CALLIPHORINAE Subfamily AMENIINAE DIAGNOSIS AND BIBLIOGRAPHY AMENIINAE Brauer and Bergenstamm, 1889 Medium-sized or large, usually metallic, Calliphoridae characterized as follows : Primary characters : Metathoracic spiracle with characteristic group of strong hairs on anterior lappet (Text-fig. 8), anterior lappet a little narrower than posterior one. Postabdomen of female not forming an extensible telescopic ovipositor. Weak convex postscutellum developed, showing trace of median incision and micro-rugose. Head almost always with very large facial carina. Additional characters : Eyes bare. Parafacials bare. Arista long plumose. Subalar bulla bare. Supra- squamal ridge bare. Lateral declivity of postalar callus densely long haired. Supraspiracular convexity bare. Propleuron and prosternum almost always setulose. Prostigmatic seta present. Prothoracic spiracle always dark brown. Stem-vein of wing bare. Vein M bent angularly forwards. Abdominal sternites very broad and exposed, in female almost always with spinous setae and often in male. Male hypopygium as in Calliphorinae. Immature stages and biology : Almost unknown. Probably larvae parasitic in land snails (Mollusca), females larviparous and retaining larvae in utero to near maturity. Larvae and puparium undescribed. Distribution (map 2, p. 136) : Oriental and Australasian Regions, excluding Tasmania and New Zealand. Eastward distribution ending abruptly at Bismarck Archipelago, absent from Solomon Islands and other Pacific islands. Unknown from Ceylon but possibly occurring there. Type-genus : Amenia Robineau-Desvoidy, 1830. AMENIIDAE Brauer and Bergenstamm, 1889, Denkschr. Akad. Wiss., Wien 56 : 81, 150, 151. Brauer and Bergenstamm, 1891, Denkschr. Akad. Wiss., Wien 58 : 309, 398. Brauer and Bergenstamm, 1893. Denkschr. Akad. Wiss., Wien 60 : 109. 46 R. W. CROSSKEY AMENIINI Malloch, 1927, Proc. Linn. Soc. N.S.W. 52 : 342. Malloch, 1928, Proc. Linn. Soc. N.S.W. 53 : 329, 614. Malloch, 1929, Proc. Linn. Soc. N.S.W. 54 : 285. Malloch, 1930, Proc. Linn. Soc. N.S.W. 55 : 101. van Emden, 1950, Entomologist's mon. Mag. 86 : 189, 196. van Emden, 1953, Entomologist's mon. Mag. 89 : 120. Paramonov, 1957, Ann. Mag. nat. Hist. (12) 10 : 52. [Ameniini + Parameniini] Enderlein, 1936, Veroff. dtsch.KolonMus. Bremen 1 : 398, 436, 446. AMENIINAE Malloch, 1933, Proc. Linn. Soc. N.S.W. 58 : 74. Mesnil, 1939, Essai sur les Tachinaires : 22, 50. Mesnil in Lindner, 1944, Flieg. Palaearkt. Reg. &4g : 18, 20. Hardy, 1951, Entomologist's mon. Mag. 87 : 96. KEY TO THE TRIBES OF AMENIINAE Head with a very strong facial carina separating antennae. Hind tibia with a pv apical seta. Outer posthumeral seta* situated mesad of presutural seta (Text- fig. 9) AMENIINI Head without a facial carina. Hind tibia without a definite pv apical seta. Outer posthumeral seta* situated laterad of presutural seta (Text-fig. 10), or sometimes about in line with it PARAMENIINI SYSTEMATIC TREATMENT Tribe AMENIINI Brauer and Bergenstamm AMENIIDAE Brauer and Bergenstamm, 1889, Denkschr. Akad. Wiss., Wien 56 : 150. DIAGNOSIS. Ameniinae with following characters : Head with facial carina. Prescutum with outer posthumeral seta situated mesad of presutural seta (Text- fig. 9). Hind tibia with PV apical seta. Prosternum and propleuron densely haired (latter occasionally bare in Stilbomyella) . Type-genus : Amenia Robineau-Desvoidy, 1830. Twelve described genera belong in the Ameniini but it is concluded from study of the type-species that only five of these can be upheld as valid, viz. Silbomyia Macquart, Platytropesa Macquart, Stilbomyella Malloch, Amenia Robineau-Desvoidy, and Formosiomima Enderlein. These genera, together with one new genus here described, can be distinguished by the key which follows. The genera Megaloprepes and Spinthemyia described by Bigot (1859) both have a setulose ventral surface to the second costal sector and other Silbomyia characters and are treated in synonymy with this genus ; Enderlein's (1936) genera Liostiria and Doleschallius are not distinguishable from Platytropesa and Stilbomyella respectively and are synonymized accordingly ; Ptylostylum of Macquart (i85ia, b) is an isogenotypic synonym of Amenia, and Neoamenia Malloch and Chaetamenia Enderlein (both with type-species not generically distinguishable from that of Amenia} are placed in synonymy with Amenia. * This seta occasionally absent on one or both sides. REVISION OF THE AMENIINAE 47 The affinities of the recognized genera of Ameniini are discussed under the appro- priate generic headings. Platytropesa and Stilbomyella are superficially similar and future discovery of new species may break down the generic distinction maintained in this paper, but for the present it appears best to treat them as separate genera. Distribution. Range of tribe coincident with that of Ameniinae as a whole. KEY TO THE GENERA OF AMENIINI Ventral surface of costa setulose between apices of veins Sc and R1 (Text-fig. 23). Scutellum with a pair of very strong erect spiniform preapical setae, set close together just dorsad of the cruciate apical setae. Fore tibia with two strong pv setae (except in timorensis) . Frons of $ very broad and equal in width to that of $ ; $ always with very strong outer vertical, pre vertical and proclinate orbital setae, as in $. [Oriental Region except for one species in Queensland] SILBOMYIA Macquart (p. 50) Ventral surface of costa bare between apices of veins Sc and R1 (Text-fig. 22). Scutel- lum without erect spiniform preapical setae. Fore tibia with one submedian pv seta. Frons of $ sometimes broad as in $, but <$ eyes often very strongly approxi- mated ; (J with or without outer vertical, prevertical and proclinate orbital setae. [Australasian Region] ........... 2 Gular region of head strongly swollen, prominent and conspicuous in profile (Text- fig. 24). Hind coxa bare on postero-dorsal surface. Middle part of anterior surface of mid femur with one strong isolated seta. Vibrissae of $ inserted level with or slightly below epistomal margin (Text-fig. 13), directed upwards and inwards. $ frons broad as in $, with outer vertical, prevertical and proclinate orbital setae PARAPLATYTROPESA gen. n. (p. 98) Gular region of head normal, not prominently swollen and visible in profile. Hind coxa setulose on postero-dorsal surface externally (bare in some specimens of Stilbomyella). Middle part of anterior surface of mid femur almost always with a group of two or more strong setae clearly differentiated. Vibrissae of <$ inserted well above level of epistomal margin (Text-fig. 14), directed more or less horizontally and crossed. <$ frons narrower than that of $ (except in Platytropesa), although eyes not always strongly approximated, N. Celebes, Rurukan, 900 m., 1.1931 (G. Heinrich} (Zool. Mus. Humb. Univ. and Staatl. Mus. Stuttgart) ; i ?, Enrekang, 5.ix.i93O (G. Heinrich} (Zool. Mus. Humb. Univ.) ; i <£, Minahassa, Tomohon, 3o.v.-2.vi.i954 (A H. G. Alston} (B. M. Nat. Hist.) ; i $, Tondano (Forster) (Rijksmus, Leiden). Distribution : Confined to Celebes, where it occurs together with S.fulgida (Bigot). Enderlein (1936, p. 440) has referred to some of the material listed above under the name 5. prospera (Walker). AFFINITIES. Allied to S. philippinensis sp. n. but easily distinguished by the characters given in the key ; also showing fairly close affinity with S. fulgida (Bigot) but readily differentiated from this species by the dark brown face and antennae, dark green metallic upper parafrontals, black-haired genae and proportions of head structures. Silbomyia philippinensis sp. n. DIAGNOSIS. Genal hair black ; upper parafrontals dark metallic greenish to violet ; interfrontal area at narrowest equal in width to or only a little wider than parafrontal at its broadest ; dorsum of thorax pollinose marginally. cJ. Head : Interfrontal area reddish brown ; ocellar area metallic greenish or greenish violet ; upper parts of parafrontals from level of lower proclinate orbital setae to vertex dark metallic green to violet in colour and without pollinosity, contrasting with creamy whitish pollinose lower parts of parafrontals ; lower halves of parafrontals and all of parafacials pale yellow in ground colour and densely yellowish white or creamy yellowish pollinose ; facial carina, antennal foveae and epistome brown or pale brown at least in part (facial carina and part of epistome sometimes yellowish), with thin inconspicuous whitish pollinosity ; genae variable REVISION OF THE AMENIINAE 59 in material seen, colour ranging from yellow with golden pollinosity to dark slightly metallic violaceous with whitish pollen ; postorbits densely white or yellowish white pollinose, the pollinosity extending dorsally more or less to the outer vertical setae. Hair of parafrontals and genae entirely black. Upper occiput slightly metallic dark green or violet, metallic appearance slightly obscured by thin white pollinosity more obvious in some lights than others ; cerebrale semi-translucent orange medially but slightly metallic blackish green or violaceous laterally. Vertex seen from above obviously narrower than one eye, eye-vertex-eye ratio about 6:5:6. Interf rental area at its narrowest point equal in width or only very slightly broader (1-2 times as wide) than one parafrontal at the corresponding point, parafrontals therefore unusually broad in relation to the interf rental area. Facial carina short and rather ridge-like, not fusiform or noticeably laterally compressed, about equal in length to distance from lunula to anterior ocellus and about 2-8-3-4 times as long as epistome. Gena about one-seventh (0-14- 0-15) of eye-height. Parafacial 2-5 times as wide as third antennal segment. Fine hairs above vibrissae reaching at most only one third of way up facial ridges. Postocellar setae fine and weak, sometimes only minute hairs. Antennae brown except for extreme base of third segment narrowly orange, third segment 3-3-3-7 times as long as second segment ; bristle on second segment exceptionally long and strong, as long as or even longer than entire antenna ; arista equal in length to third antennal segment. Palpi yellow or brownish yellow. Thorax : dorsum varying from bluish green occasionally with small violaceous patches to deep bluish violet (as in holotype), the prescutum, notopleura and areas of supra-alar setae with a covering of white pollinosity which is most easily seen in posterior view ; sides of thorax mostly bluish green, the mesopleura and sternopleura with the usual very large densely white pollinose spots ; hypopleura and posterior parts of pteropleura reddish brown with metallic reddish violaceous reflections. Wings : with heavy brown infuscation broadly along the veins, darkening appear- ing most concentrated anteriorly where the veins are close together, wing membrane very pale brownish in cells and along hind margin. Distance between bend of vein M and wing margin i -6-1 -8 times as great as that between m-cu and bend ; on vein M distance from r-m to m-cu 2-7-3-3 times that between m-cu and bend. Costal spine short and inconspicuous, shorter than r-m. Margin of lower calypter dark brown, calyptrae otherwise white. Legs : black, femora with bluish green to violaceous metallic reflections. Abdomen : bluish green to violet, deep bluish violet in holotype specimen. T3 on entire dorsum and medially on ventro-lateral surfaces with a covering of white pollinosity, very conspicuous in posterior view ; T4 without pollinosity ; T5 with a pair of very large and very conspicuous white pollinose spots which extend from extreme ventral margins of the tergite round to the latero-dorsal surfaces, the spots easily seen from above. Ti + 2 with a pair of strong median marginal setae ; T3 with a single lateral marginal seta on each side ; T3 with a pair of median discal setae, usually strong but one sometimes shorter and weaker than the other. Hair of dorsum of T3 erect and rather long spiniform on median third, semi-recumbent and finer laterally ; hair of T4 semi-erect on most of the dorsum, sometimes very slightly spiniform near the middle of the tergite but usually shorter and finer than that on T3 ; hair of T5 very fine and erect. <$ hypopygium very similar to that of S. albonotata (Text-fig. 32). Measurements : body length 13-1 mm. (range 11-6-15-5 rnm.) wing length 12-2 mm. (range 11-3-14-2 mm.) [5 specimens] : maximum measurements given are those of holotype. $. Almost identical with <$ except for very slightly broader parafacials and genae and vertex almost equal in breadth to one eye when measured from above. Measurements : body length 14.4 mm. (range 12-2-15-8 mm.), wing length 12-6 mm. (range 10-0-14-2 mm.) [4 specimens]. MATERIAL EXAMINED. Holotype £, PHILIPPINE ISLANDS : Luzon, Mt. Makiling (Baker). In British Museum (Natural History), London. Paiatypes : PHILIPPINE ISLANDS : 2 <$<$, i ?, Luzon, Mt. Makiling (Baker) (U.S. Nat. Mus.) ; i $ Luzon, Mt. Makiling (Baker) (B. M. Nat. Hist.) ; i $, Baguio, Benguet [? Luzon or Mindanao] (Baker] (U.S. Nat. Mus.) ; i $ Mindanao, Surigao (Baker) (U.S. 60 R. W. CROSSKEY Nat. Mus.) ; i , Mindanao, Kolambugan (Baker) (U.S. Nat. Mus.) ; i , Balokambong, Tjiletoch Bay, viii.ig37 (B.M. Nat. Hist.) ; 8 $$, 3 $?, Soekaboemi, iii-vii.i926 (E. le Moult] (B.M. Nat. Hist.) ; i , data as for lectotype (D. Ent. Inst.) ; i , Yamo no Taiko, ix.igoS (H. Sauter} (D. Ent. Inst.) ; 3 £?, Kanshizei, v.igoS (Sauter} (D. Ent. Inst. & B.M. Nat. Hist.) ; i , Takao, ix.igoy (H. Sauter} (Zool. Mus. Humb. Univ.) ; i ^, i $, Toyen- mongai bei Tainan, v.igio (Rolle) (Zool. Mus. Humb. Univ.) ; i $, 3 , Kosun, v.igoS (Sauter} (D. Ent. Inst.) ; i $, Koshun, v.igoS (Sauter) (B.M. Nat. Hist.) ; 1 c£, i $, Koshun, viii.igoS (Sauter) (D. Ent. Inst.) ; i °-, Kankau, Koshun, 7.xi.igi2 (H. Sauter) (D. Ent. Inst.) ; i $, Kankau, Koshun, 7.viii.i9i2 (H. Sauter) (Zool. Mus. Humb. Univ.) ; i <£, i $, Kankau, ix.igi2 (H. Sauter) (Zool. Mus. Humb. Univ.) ; i $, Formosa (Zool. Mus. Humb. Univ.). FORMOSA : 10 specimens of S. latigena labelled erroneously by Enderlein as "type" or " cotype " of " Stilbomyia sauteri End. " (7 specimens), and " Stilbomyia sauteri var. viridis End. " (3 specimens), data as follows : i $, nordl. Paiwan Distr., Faroe, 7.ix.i9i2 (H. Sauter) (D. Ent. Inst.) ; i , Takao, 19.1.1908 (H. Sauter) (Zool. Mus. Humb. Univ.) ; i $, Kosempo, 31^.1908 (H. Sauter) (Zool. Mus. Humb. Univ.) ; 2 &?, Formosa I. (Sauter) (D. Ent. Inst. & Zool. Mus. Humb. Univ.) ; 2 $$, Koshun, viii.igoS (Sauter) (D. Ent. Inst.) ; i <$, Kankau, Koshun, 7.xi.i9i2 (H. Sauter) (Zool. Mus. Humb. Univ.) ; i <£, i $, Kankau, Koshun, 7.viii. and 7.xi.i9i2 (H. Sauter) (D. Ent. Inst.). Two specimens labelled by Enderlein as " Stilbomyia latigena var. viridis — cotype Enderl. $ " (unpublished varietal name of latigena), REVISION OF THE AMENIINAE 75 data as follows : i $, Koshun, viii.igoS (Sauter) and i $, Kankau, Koshun, 7.viii.i9i2 (H. Sauter} (D. Ent. Inst). Each specimen listed above bears an identity label in Enderlein's writing. A further 30 specimens of Sauter's material have been seen which are not labelled by Enderlein ; there is no evidence that Enderlein saw this additional material, which I have therefore not considered to be part of the syntypic series and have not labelled as paralectotypes. Data are as follows : FORMOSA : i <$, nordl. Paiwan Distr., Faroe, x.igi2 (H. Sauter} (B.M. Nat. Hist.) ; i ?, nordl. Paiwan Distr., Paroe, 7.ix.i9i2 (H. Sauter} (D. Ent. Inst.) ; i $, nordl. Paiwan Distr., Paroe, 7.ix.igi2 (H. Sauter} (U.S. Nat. Mus.) ; 2 ??, Chipun, Puyuma Distr., vii.igi2 (H. Sauter} (D. Ent. Inst. and B.M. Nat. Hist.) ; i ?, Fuhosho, vii.igog (H. Sauter} (D. Ent. Inst.) ; i $, Kosempo, iv.igoS (H. Sauter} (D. Ent. Inst.) ; i $, Kanshirei, v.igoS (H. Sauter) (D. Ent. Inst.) ; i & Formosa I. (Sauter) (D. Ent. Inst.) ; 2 $$, i ?, Sokutsu, ix.igi2 (H. Sauter) (D. Ent. Inst. and B.M. Nat. Hist.) ; i <£, Tainan, iv.igio (Sauter) (D. Ent. Inst.) ; i $, Koshun, vii.igog (Sauter) (D. Ent. Inst.); 1 cJ, Koshun, vii.igoS (Sauter) (B.M. Nat. Hist.) ; i $, Koshun, 7.viii.igi2 (H. Sauter) (B.M. Nat. Hist.) ; 2 ? (Sawter) (Zool. Sammlung. Munich). Other material : FORMOSA : 4 ?$, is.x.igio (H. Rolle) (B.M. Nat. Hist.) ; i ?, Koannania, 22.vii.igo8 (B.M. Nat. Hist.) ; i ?, N. Formosa, Kushaku, v.igo3 (Haberer) (Zool. Sammlung. Munich) ; 3 $$, Tainan (B.M. Nat. Hist., Zool. Sammlung. Munich and Staatl. Mus. Stuttgart) ; i ?, " Japan ", Formosa, Shinkwa, i6.x.ig26 (S. Takano) (U.S. Nat. Mus.) ; i $, Formosa (no other data) (ex coll. Brunetti) (B.M. Nat. Hist.). Distribution : 5. latigena is confined to the island of Formosa, where it is evidently common and occurs in company with the closely related S. sauteri Enderlein. The specimen collected by the Japanese dipterist Professor Takano, now in the U.S. National Museum and labelled " JAPAN, Formosa, Shinkwa ", is from Formosa ; it was collected in ig26 when Formosa formed part of the Japanese Empire and the word " Japan " on the label indicates that the specimen was collected in one of the then Japanese islands. The genus Silbomyia is absent from Japan. AFFINITIES. Most closely allied to 5. fuscipennis and 5. sauteri. From 5- fuscipennis it is distinguished by the venational characters mentioned in the key, and also by the shorter facial carina and antennae, and broader vertex ; the abdomen also differs from that in S. fuscipennis, there being no white pollinosity on T4, and the hair on T5 being erect (in $ erect also in middle of T3 and T4), whereas the abdominal hair in 5. fuscipennis is entirely recumbent. 5. latigena is easily distin- guishable from S. sauteri by the yellow or silvery yellow pollinose postocular stripe (all bright silver in sauteri}, by the much longer more fusiform facial carina and longer $ antennae, and by the absence of median discal setae on T3 and T4 of the abdomen (such setae normally present in sauteri}. The differences from S. sauteri apply also to S. hoeneana Enderlein. 76 R. W. CROSSKEY Silbomyia sauteri Enderlein, 1936 Stilbomyia sauteri Enderlein, 1936, Veroff. dtsch. KolonMus. Bremen 1 : 439. Lectotype , Kanshizei, v.igoS (Sauter) (D. Ent. Inst.) ; i <£, 2 $$, Formosa (no other data) (ex. coll. Brunetti} (B.M. Nat. Hist.) ; i <$, Formosa I. (Sauter) (D. Ent. Inst.) ; 2 $$, Suisharyo, x.igii (Sauter) (B.M. Nat. Hist. & D. Ent. Inst.) ; 3 $<$, Tainan (Zool. Sammlung, Munich & B.M. Nat. Hist.) ; 2 $$, i $, Formosa (Sauter} (Zool. Sammlung, Munich) ; i $, Formosa (Sauter} (Staatl. Mus. Stuttgart) ; i $, Koshun, viii.igoS (Sauter} (B.M. Nat. Hist.) [green specimen] ; i $, Suisharyo, x.igii (H. Sauter} (D. Ent. Inst.) [green specimen] ; i $, Paroe, nordl. Paiwan Distr., 7.ix.i9i2 (H. Sauter) (D. Ent. Inst.) [green specimen]. Note : 10 specimens labelled by Enderlein as ' type ' or ' cotype ' of S. sauteri and S. sauteri var. viridis belong to S. latigena Enderlein and are therefore listed among the material examined of S. latigena ; these specimens are nonetheless paralectotypes of S. sauteri and 5. sauteri var. viridis. Distribution : Occurs only in Formosa, together with 5. latigena Enderlein. AFFINITIES. Very closely related to 5. hoeneana Enderlein from the mainland of China, with a very similar facial carina and silvery white postocular stripe. It is 78 R. W. CROSSKEY possible that S. hoeneana and S. sauteri are conspecific, for the morphological dis- tinctions are certainly slight, but on the evidence available at present it appears best to recognise the two species as distinct. 5. sauteri is distinguished from 5. hoeneana by the broader interfrontal area (about three and a half times as wide as a paraf rental), by the presence in almost all specimens of median discal setae on at least one and usually both intermediate abdominal tergites, and normally by the violet-blue coloration (S. hoeneana always green in the material seen). 5. sauteri is easily distinguished from S. latigena, also from Formosa, by the short facial carina (not at all fusiform as in latigena) and silver-white postorbits. DISCUSSION. With present evidence it is not possible to accord separate syste- matic status to the green-coloured form of this species (var. viridis of Enderlein). Green specimens appear to be conspecific with the commoner violet-blue specimens, and specimens with this different coloration have been seen with identical data ; the difference is certainly not subspecific in the absence of allopatry. It is worth noting however that the wings are slightly shorter in relation to the body length in green specimens than in violet-blue specimens, the wing length being about ten- thirteenths of the body length in bright green individuals and eleven or twelve- thirteenths of the body length in blue to violet specimens. As yet there is insufficient material available to assess the significance of this apparent distinction. Silbomyia hoeneana Enderlein, 1936 Stilbomyia hoeneana Enderlein, 1936, Veroff. dtsch. KolonMus. Bremen 1 : 439. Lectotype <$, CHINA. In the Zoologisches Museum der Humboldt-Universitat, Berlin. LECTOTYPE DESIGNATION : the available type-material of S. hoeneana comprises eight syntypes collected by Dr. Mell in China, seven labelled by Enderlein as ' Type ' and one (in Staatl. Mus. Stuttgart) as ' Cotype '. A ^ syntype in Zool. Mus. Humb. Univ. has been labelled and is here designated as lectotype, and the other syntypes have been labelled as paralectotypes (three in Zool. Mus. Humb. Univ., two in B.M. Nat. Hist, and one in D. Ent. Inst.). In the original description Enderlein mentions two specimens from Nanking in addition to the material collected by Dr. Mell ; the whereabouts of these two syntypes has not been traced. DIAGNOSIS. Very similar to S. sauteri but lacking median discal setae on inter- mediate abdominal tergites. cJ. Head : Interfrontal area orange or orange-yellow ; parafrontals, parafacials, facial ridges, antennal foveae, facial carina, epistome and genae yellow with golden yellow pollinosity ; postorbits with blackish ground colour and dense silvery pollinosity conspicuously contrasting with yellow genae. Parafrontal hair black, hair of genae long and yellow. Upper occiput dark greenish metallic in certain lights, thinly whitish pollinose ; cerebrale orange. Eye-vertex-eye ratio about 5:7:5. Interfrontal area very broad, 3'3-3'5 times as wide as a parafrontal at level of lower proclinate orbital seta. Facial carina short and broad, rather ridge-like and not at all fusiform, carina slightly shorter (0-9) than distance from lunula to anterior ocellus and 2-8-3-0 times as long as epistome. Gena about two-ninths (0-22) of eye-height. Parafacial two and a half times as wide as third antennal segment ; facial ridges distinctly concave in profile with fine hairs above vibrissae confined to lower quarters. Postocellar setae usually strongly de- veloped, sometimes two pairs. Antennae pale orange, third segment 3'7~3'9 times as long as REVISION OF THE AMENIINAE 79 second segment ; seta on second segment long and strong, about as long as arista ; arista much longer than third antennal segment. Palpi yellow. Thorax : mesonotum usually emerald- green, occasionally with cupreous reflections, violaceous blue in one specimen seen ; scutellum sometimes more bluish than mesonotum ; sides of thorax green or bluish green, hypopleura and pteropleura more reddish brown with metallic greenish reflections. Dorsum with white pollinosity, conspicuous seen from behind, on humeral calli, notopleura, areas of supra-alar setae, prescutum and postalar calli. Mesopleura and sternopleura with usual large densely pollinose white spots. Wings : dark brown infuscate, the infuscation distinctly weaker in centres of cells and along hind margin. Distance from bend of vein M to wing margin 1-5-1-7 times as great as that between bend and m-cu ; on vein M distance from r-m to m-cu 2-6-3-5 times as great as that between m-cu and bend. Costal spine distinct, a little shorter than r-m. Margin of lower calypter dark brown, calyptrae otherwise white. Legs : black, femora with dark greenish metallic reflections. Abdomen : usually unicolorous with dorsum of thorax occasionally slightly more blue, colour usually emerald green but sometimes greenish blue, violet in one specimen seen. T3 with white pollinosity on most of dorsum, conspicuous from behind, the pollinosity extending round the sides of the tergite to form conspicuous silvery white median bands ventro-laterally ; T4 non-pollinose ; T5 with a pair of large white pollinose areas ventro-laterally which extend round sides of tergite just on to dorsum, appearance of these spots shifting with the light. Ti + 2 without median marginal setae ; T3 with a variable number of lateral marginal setae on each side, usually two but occasionally three or four, sometimes one strong seta and one much weaker one ; T3 and T4 without median discal setae. Hair of T3 and T4 sometimes mostly recumbent but sometimes almost all semi-erect or erect, conspicuously thickened and spiniform on median dorsal area of each intermediate tergite ; hair of T5 long and erect, sometimes very slightly spiniform but always finer than on preceding tergites, o* hypopygium as in S. sauteri (Text-fig. 33). Measurements : body length 14-6 mm. (range 12-9-16-8 mm.), wing length 12-4 mm. (range 10-5-14-9 mm.) [n specimens]. $. Very similar to 6*. antennae and facial carina not noticeably sexually dimorphic. Gena and parafacial broader than in $, former about one-third (0-33-0-36) of eye-height, latter about three and a half times as wide as third antennal segment. Measurements : body length 15-0 mm. (range 13-2-17-4 mm.) ; wing length 13-4 mm. (range 11-7-15-9 mm.) [18 specimens]. MATERIAL EXAMINED. Lectotype $, CHINA : Canton, Tsha-jiu-san, i^.vii.igio (S. V. Mell). Paralectotypes : CHINA : i $, Canton, Tsha-jiu-san, I4.vii.igio (S. V. Mell) (B.M. Nat. Hist.) ; i $, i ?, Tsha-jiu-san, vii-vm.igio (S. V. Mell) (Zool. Mus. Humb. Univ.) ; 2 $?, Canton (S. V. Mell) (D. Ent. Inst. & Zool. Mus. Humb. Univ.) ; 2 $$, Canton (S. V. Mell) (B.M. Nat. Hist. & Staatl. Mus. Stuttgart). CHINA : i $, Canton, I4.vii.i9io (Zool. Sammlung. Munich) ; i $, Kiukiang, vii.i887 (Pratt) (B.M. Nat. Hist.) ; i , MALAYA : Malacca, Quedah (v. d. Does de Bye] (Rijksmus. Leiden). Distribution : South-east Asia from India to Malaya. AFFINITIES. 5. asiatica sp. n. appears to be most closely related to S. hoeneana Enderlein and S. metallica sp. n. ; from hoeneana it is distinguished by the white margin to the lower calypter, by the narrower interfrontal area and smaller size, and from metallica by the much broader interfrontal area. From both these species it also differs in the shining creamy whitish appearance of the parafacials when seen from above. There is some resemblance to S. sumba sp. n. but 5. asiatica sp. n. is at once distinguished from this species by the absence of median marginal setae on Ti + 2 and by the shorter facial carina and antennae. Silbomyia metallica sp. n. DIAGNOSIS. Ti + 2 without median marginal setae ; parafrontals unusually broad and interfrontal area only 1-4-1-7 times as wide as paraf rental at level of lower proclinate orbital seta ; margin of lower calypter white ; dorsal surfaces of T4 and TS under high power examination completely smooth and brilliantly metallic. $. Head : Interfrontal area orange-yellow ; vertex and upper parts of parafrontals semi- translucent yellowish or orange-yellow, rather shining and scarcely at all pollinose ; lower parts of parafrontals, parafacials, genae, facial carina, antennal foveae and epistome yellow or orange yellow, pollinosity golden on lower parafrontals, parafacials and genae but thinner and paler yellowish on face ; postorbits densely silvery white pollinose, the pollinosity reaching to outer vertical setae and extreme upper ends of postorbits not at all metallic. Parafrontal hair 82 R. W. CROSSKEY all black ; hair of genae golden yellow. Upper occiput thinly whitish pollinose, but appearing metallic green in some lights ; cerebrale orange. Vertex almost exactly equal in width to one eye seen from above, eye-vertex-eye ratio about 13 : 12 : 13. Interfrontal area 1-4-1-7 times as wide as a parafrontal at level of lower proclinate orbital seta, parafrontals therefore unusually broad and interfrontal area relatively narrow. Facial carina short and ridge-like, slightly widening ventrally, only 2-5-2-8 times as long as epistome and distinctly shorter than distance from lunula to anterior ocellus. Gena relatively broad, nearly one-third (0-31) of eye-height. Parafacial three times as wide as third antennal segment. Fine hairs above vibrissae confined to lower quarter of each facial ridge, facial ridges slightly but distinctly concave in profile. Postocellar setae weakly developed. Antennae orange, third segment 3-3-3-5 times as long as second segment ; seta on second segment long and strong, almost as long as whole antenna and longer than arista, latter longer than third antennal segment. Palpi yellow. Thorax : brilliant green with slight coppery or bluish tinge, mesopleura and sternopleura with usual large white spots of dense pollinosity ; hypopleura and pteropleura reddish brown with violaceous reflections ; mesonotum when viewed from behind showing very thin inconspicuous traces of whitish pollinosity around the margins, the pollinosity much less obvious than in other species in which such pollen is present. Wings : heavily infuscate very dark brown along the veins and paler brownish in cells and posteriorly. Distance between bend of vein M and wing margin 1-6 times as great as between m-cu and bend ; on vein M distance from r-m to m-cu 2-7-2-9 times as great as that between m-cu and bend. Costal spine small, much shorter than r-m. Calyptrae white, including posterior and outer margins of lower calypter. Legs : black, femora partly dark metallic bluish green. Abdomen : bright metallic green, somewhat coppery posteriorly and on ventral surface with broad violaceous hind margins to the tergites. Dorsal surfaces of T4 and T5 under high magnification quite smooth and polished, exceptionally brilliantly shining. T3 with a conspicuous broad median band of white pollinosity on latero- ventral surfaces, but with no white pollinosity visible on dorsum from any point of view ; T5 with usual pair of conspicuous spots of dense white pollinosity, mainly ventral in position but extending on to extreme sides of the tergite. Ti + 2 without median marginal setae ; lateral marginal setae of T3 single on each side ; T3 and T4 without median discal setae. Hair of dorsum entirely recumbent, including that on T5. Measurements : body length 11-7 mm. (range 10-9-12-6 mm.), wing length 10-5 mm. (range 9-8-11-2 mm.) [4 specimens]. $. Unknown. Probably very similar to $>• MATERIAL EXAMINED. Holotype $, INDONESIA : E. Borneo, Babidjoelan, approx. 4,000 ft., vi.i937. In British Museum (Natural History), London. Paratypes : 3 $$, data and depository as for holotype. Distribution : At present known only from the four female specimens of the type-series from Borneo, and probably confined to Borneo where no other species of Silbomyia is known to occur. AFFINITIES. S. metallica sp. n. appears to be most closely allied to 5. fulgida (Bigot) and 5. sumba sp. n. ; it is easily distinguished from both these species by the lack of median marginal setae on Ti +2 by the proportions of the interfrontal area and parafrontals, by the white margin of the lower calypter, and by other minor differences. FIGS. 24-30. 24. Head of Paraplatytropesa gen. n. in profile showing prominent gular development. 25. Abdominal shape in Amenia. 26. Abdominal shape in Stilbomyella. 27. Abdomen of Formosiomima nigromaculata (Malloch) showing arrangement on T.4 of separated pairs of marginal setae, remarkable pattern of black spots and weakness of sutures between tergites. 28. Profile of abdomen of $ Platytropesa auriceps Macquart. Figs. 29 and 30. Sternite 5 of $ of (29) Platytropesa simulans sp. n. and (30) Platytropesa auriceps Macquart. REVISION OF THE AMENIINAE T5 29 30 84 R. W. CROSSKEY PLATYTROPESA Macquart, 1851 Platytropesa Macquart, 1851, Mem. Soc. Sci. Lille, Annee 1850 : 197, and Dipteres Exot. Suppl. 4 : 224. [Spelling Platytropeza in Dipteres Exot. Suppl. 4, Index : 357]. Type-species : Platytropesa auriceps Macquart, 1851 [— ruriceps, by typographical error], by monotypy. Liostiria Enderlein, 1936, Veroff. dtsch. KolonMus. Bremen, 1 : 440. Type-species : Liostiria ralumensis Enderlein, 1936 [= Stilbomyella dubia Malloch, 1935], by original designation. syn. n. DIAGNOSIS. Ventral surface of costa bare between apices of veins Sc and Rt. Head normal, gular region not produced. Fore tibia with one submedian pv seta and with two small pd setae (Text-fig, n). Mid femur with two or more strong submedian a setae. Hind coxa setulose on postero-dorsal surface. Facial ridges with fine setulae extending more than half way (<£) or about half way ($) up their length. Facial carina very strongly sexually dimorphic. Frons about equal in width in both sexes, <$ eyes not approximated ; <§ with outer vertical, prevertical and sometimes proclinate orbital setae. Inner vertical setae cruciate. Abdomen with- out white pollinose spots on T5. Sternites of <$ abdomen with very long dense hair (Text-fig. 28), sternites of $ abdomen with spinous setae. DISCUSSION. Platytropesa is to some extent intermediate between Silbomyia Macquart and Stilbomyella Malloch, but the general facies and the long dense hair on the sternites of the <$ suggest closer affinity with the latter genus ; the bare ventral surface of the costa between the apices of Sc and /?x easily distinguishes Platytropesa from Silbomyia, but it agrees with this genus in the broad <$ frons with outer vertical and prevertical setae and in having small pd setae on the fore tibia. The latter character distinguishes Platytropesa from Stilbomyella and Paraplaty- tropesa gen. n., both of which lack pd setae on the fore tibia ; the normal gular region of the head distinguishes it from Paraplatytropesa. There is confusion in the literature concerning the name and type-locality of the type-species of Platytropesa. Macquart (1851) spelled the name ruriceps in the original description and cited the type-locality as " Oceanic, Triton Bay ". Towns- end (1931) pointed out that the type was labelled " auriceps " and therefore attributed the original spelling " ruriceps " to a typographical error ; the spelling " ruficeps " in Macquart's (1851) Index p. 357 to the 4th Supplement of his Dipteres Exotiques is also a misprint. It appears certain that Macquart's name alluded to the golden yellow head, a character mentioned in his original description (' Tete d'un jaune dore '), and Townsend's (1931) emendation to auriceps is justified, especially as the type is labelled " Platytropesa auriceps $, n.g., n. sp., Macq." in Macquart's writing. There is therefore no evidence to support Paramonov's (1957, p. 62) emendation, based on remarks of Se"guy, to rubriceps. Triton Bay, type-locality of auriceps, lies on the southern coast of the narrow western ' neck ' of New Guinea, an area where P. auriceps will probably prove to be quite common when sufficient collecting has been done. Townsend (1935, 1937) erroneously, and without any explanation, cited the type-locality of auriceps as the Paracel Islands, and Enderlein (1936, p. 445) repeated this mistake. Platytropesa is not known from the Paracel Islands in the China Sea or from anywhere near there, REVISION OF THE AMENIINAE 85 and Macquart's original citation of Triton Bay quite certainly means the inlet still known by that name in western New Guinea. DISTRIBUTION (map i, p. 123). Platytropesa occurs throughout New Guinea and its neighbouring islands, including Morotai in the Moluccas, Misool, Waigeo, Biak, the Aru Islands, and the Bismarck Archipelago (New Britain and New Ireland) ; it occurs also in northern Queensland, including Palm Island. It is not yet known from Halmahera, Ceram, and Obi but almost certainly occurs in these islands of the Molucca group. KEY TO THE SPECIES 1 Head in facial view with inner margins of eyes slightly but distinctly angulate near level of lunula (Text-fig. 16). Lower calypter dark brown on about apical fifth (<$} or quarter ($). Mesolobe of $ hypopygium curved in profile and rounded at tip (Text-fig. 39). Hair of $ sternite 5 very long and largely curved downwards and inwards apically (Text-figs. 28 and 30). $ facial carina 5-3-6-8 times as long as epistome. <$ with or without proclinate orbital setae ..... 2 Head in facial view with inner margins of eyes slightly but evenly curved, not at all angulate (Text-fig. 15). Lower calypter dark brown on about apical third to two-fifths ($) or half ($). Mesolobe of $ hypopygium rather straight in profile, slightly truncate apically with trace of hook (Text-fig. 38). Hair of <$ sternite 5 shorter and not conspicuously turned downwards or inwards apically (Text-fig. 29). (J facial carina 4-5-4-8 times as long as epistome. <$ without proclinate orbital setae ........ P. simulans sp. n. (p. 89) 2 Mesopleuron shining, without large white pollinose spot. <$ without or with one pair of proclinate orbital setae. [Bismarck Archipelago] . . P. dubia (Malloch) (p. 88) Mesopleuron not shining, mostly covered by large densely white pollinose spot. <$ always with two pairs of proclinate orbital setae [not known from Bismarck Archi- pelago] ........ P. auriceps Macquart (p. 85) DESCRIPTIONS OF THE SPECIES Platytropesa auriceps Macquart, 1851 (Text-figs. 16, 28, 30, 39, 42) Platytropesa ruriceps [sic] Macquart, 1851, M&m. Soc. Sci. Lille, Annee 1850 : 197. Dipteres Exot. Suppl. 4 : 224. Holotype £ (not $ as cited by Macquart), TRITON BAY (NEW GUINEA). In the Museum National d'Histoire Naturelle, Paris. [Erroneous spelling of auriceps by typographical error.] Musca opulenta Walker, 1859, /. Linn. Soc. Lond. (Zool.) 3 : 104. Holotype $, ARU ISLANDS. In the British Museum (Natural History), London, syn. n. Silbomyia decrescens Walker, 1864, /. Linn. Soc. Lond. (Zool.) 7 : 215. Holotype (J, MYSOL (= MISOOL). In the British Museum (Natural History), London, syn. n. Platytropesa auriceps Macquart, Townsend, 1931, Ann. Mag. nat. Hist., 10 (8) : 376. [Justified emendation of ruriceps Macquart.] [Stilbomyia costalis (Walker) ; Malloch, 1930, Proc. Linn. Soc. N.S.W., 55 : 102, [not of Walker] (misidentification)] . DIAGNOSIS. Mesopleuron with large white pollinose spot ; lower calypter dark brown only on posterior quarter or less ; inner eye-margins in facial view slightly angulate near level of lunula ; $ with two pairs of proclinate orbital setae. 86 R. W. CROSSKEY o*. Head : Interf rental area dark brown or dark reddish brown ; vertex and ocellar plate dark metallic greenish or bluish, yellow pollinose on either side of posterior part of ocellar plate ; parafrontals, parafacials, genae and postbuccae densely pale yellow to deep golden yellow pollinose over yellow ground colour ; antennal foveae and epistome yellow with thin whitish pollinosity ; facial carina yellow with moderately thick shining pale yellow pollinosity on flattened anterior surface ; postorbits thickly pale yellow to deep golden pollinose ; occiput with dark greenish or bluish ground colour thickly covered with yellow pollinosity, metallic coloration only slightly exposed near cerebrale. Parafrontal hair long and fine, all pale to dark brown ; hair of entire occiput, postbuccae and genae yellowish white to golden yellow. Inner margins of eyes in facial view slightly but distinctly angulate (fig. 16) near level of lunula ; vertex slightly less than a quarter of total head width, eye-vertex-eye ratio about 5 13 : 5. Ocellar and cruciate frontal setae all strongly developed ; parafrontals with two pairs of strong proclinate orbital setae. Facial carina very long and heavy, its anterior surface broad and flattened but tapering strongly in upper third towards lunula, sides of the carina very strongly pinched-in towards one another so that antennal foveae are extremely deep, the carina about twice as long as distance from lunula to anterior ocellus and 5-3-6-8 times as long as epistome; in profile the carina gently convex and abruptly set off from the epistome, latter short and slightly prominent. Gena about three-tenths (0-29-0-31) of eye-height. Parafacial set off at very sharp angle from inner eye margin, about equal in width to third antennal segment ; in facial view parafacial appearing very narrow, only about as wide as antenna in facial view. Facial ridges in profile nearly straight, fine setulae reaching slightly over half way up each ridge. Antennae inserted far above mid-eye level, in profile very largely hidden within very deep foveae ; antennal colour blackish brown or very dark reddish brown, third segment extremely elongate and 7-7-8-9 times as long as second segment; seta on second segment short, fine and weak ; arista thickened on basal two-thirds, densely plumose and about three-quarters as long as third antennal segment. Palpi yellowish brown. Thorax : usually brilliant emerald green, occasionally with slight coppery tinge ; sometimes violaceous blue with violet scutellum. Hypopleural and posterior pteropleural regions largely reddish brown with metallic greenish or violaceous areas. Dorsum entirely shining metallic, without trace of white pollinose areas. Mesopleuron with a very large conspicuous densely white pollinose spot, appearance of spot shifting only slightly with direction of light ; sternopleuron with thin inconspicuous traces of white pollen visible in some lights, without definite spot. Wings : conspicuously dark brown infuscate anteriorly and broadly towards the base, infuscation fading posteriorly but all of the wing with at least a very faint trace of darkening (wing not abruptly divided into a dark costal band and clear posterior region as in Stilbomyella] . Lower calypter dark brown only on posterior quarter or fifth, otherwise white. Legs : black, femora with brilliant metallic green or violaceous reflections. Mid tibia with two strong ad setae. Abdomen : unicolorous with thorax, varying from brilliant metallic green to violet ; sometimes with slight copper tinge. Margins of tergites dorsally appearing slightly darkened to naked eye, ventrally the tergite margins very narrowly but obviously blackish violet. No trace of white pollen spots anywhere on abdomen, but seen from behind the dorsum of T3 shows exceedingly thin trace of pollinose covering and also trace of a black median vitta ; median excavation of Ti + 2 usually blackish. Ti + 2 without median marginal setae ; T3 with a pair of very long strong median marginal setae ; tergites without discal setae. Hair of T3 and T4 of short even length, slightly thickened and erect or semi- erect ; hair of T5 finer and erect. Venter with very long dense hair situated mainly on sternites, but hair of ventral ends of intermediate tergites also rather fine and long ; hair of sternites 3 and 4 very long and reaching back under sternite 5 ; hair of sternite 5 extremely long and dense, ends of longest hairs curling downwards (Text-fig. 28) in lateral view and also inwards towards hairs of opposite lobe of the sternite (Text-fig. 30). Ends of longest hairs of sternites very fine and crinkly. <$ hypopygium as in Text-figs. 39 and 42 ; mesolobes distinctly curved in profile and evenly rounded at extreme tips, slightly variable in length (longer and narrower in specimens from Palm Islands, Queensland, than in specimens seen from elsewhere) ; paralobes parallel- sided in profile and usually rather long, evenly curved apically. Measurements : body length 10-7 mm. (range 8-6-I3-3 mm.), wing length 8-4 mm. (range 6-7-10-1 mm.) [7 specimens]. REVISION OF THE AMENIINAE 87 $. Mostly like <£, but head in the sexes conspicuously sexually dimorphic, face and antennae not greatly elongate as in <$. Facial carina not strongly flattened on anterior surface and not strongly pinched-in laterally, antennal foveae less deep than in